I'm looking for a job. I exported this list from FewerJobs.com - a curated job board. Please: 1. Rank these jobs by fit for me, given my resume / skills. 2. Highlight the top 5 with a one-sentence rationale each. 3. Flag any concerns, including benefit values without source-backed evidence. 4. Suggest one or two filter changes I could make on FewerJobs to find more good matches. Filters I applied: - q: Acadia Pharmaceuticals Inc - quality_floor: all - match_401k_strict: true - parental_strict: true - non_birth_strict: true - pto_strict: true - include_older: false - apply_url_verified: false - page: 1 - per_page: 100 - sort: relevance Jobs (100 total): --- TITLE: Manager, Market Research EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: San Diego, California, United States (unspecified) SALARY: $113K-$142K POSTED: 2026-05-20 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8550941002?gh_jid=8550941002 EXCERPT: Manager, Market Research San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position is based in San Diego, CA. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Manager, Market Research leads the planning and execution of primary and secondary research to generate customer insights that shape commercial strategy across Acadia's therapeutic portfolio. This role partners closely with the Director of Market Research, cross‑functional stakeholders, and external vendors to support in‑market brands, pipeline development, product launches, lifecycle management, and business development initiatives. The role serves as a strategic thought partner, translating complex research findings into clear, actionable recommendations for senior leadership. Primary Responsibilities - Lead end‑to‑end qualitative and quantitative market research initiatives supporting in‑line brands and pipeline assets - Manage all phases of research execution including RFP development, vendor selection, contracting, study design, stimulus development, and project oversight - Oversee research budgets, timelines, and deliverables to ensure --- TITLE: Senior Director, Regulatory Operations EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States (unspecified) SALARY: $221K-$276K POSTED: 2026-05-27 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8558062002?gh_jid=8558062002 EXCERPT: Senior Director, Regulatory Operations Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position is based in Princeton, NJ, South San Francisco, CA or San Diego, CA. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Senior Director, Regulatory Operations provides strategic and operational leadership for global regulatory operations, overseeing electronic submissions, regulatory information management systems, and end‑to‑end submission execution. This role is a key member of the Global Regulatory Affairs Leadership Team and plays a critical role in driving operational excellence, scalability, compliance, and digital innovation across Regulatory Affairs. The position partners closely with Regulatory Affairs leadership, IT, Quality, and cross‑functional teams to ensure high‑quality, compliant, and timely submissions worldwide while advancing modern systems and emerging technologies, including AI. Primary Responsibilities - Lead and scale the global Regulatory Operations function, including organizational design, talent strategy, --- TITLE: Associate Director Toxicology EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States (unspecified) SALARY: $155K-$193K POSTED: 2026-02-23 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8426430002?gh_jid=8426430002 EXCERPT: Associate Director Toxicology Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position can be based in San Diego, CA OR San Francisco, CA OR Princeton, NJ . Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Associate Director will be responsible for the oversight of Translational Science preclinical safety assessment/toxicology deliverables, with a clear understanding of functional interdependence and critical path activities. The role will contribute to the research and/or development of the products, projects, and programs in support of the pipeline. Collaborate cross‑functionally to conduct basic research and development, including designing and overseeing preclinical safety and toxicology studies in support of diverse projects and long-term company objectives. Ensure timely and effective communication of project status and issues to drive alignment and successful completion of team goals and deliverables. Primary Responsibilities - Plans experimental safety --- TITLE: Associate Director Clinical Operations EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States (unspecified) SALARY: $148K-$185K POSTED: 2026-04-17 K401_MATCH: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8510279002?gh_jid=8510279002 EXCERPT: Associate Director Clinical Operations Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position can be based in Princeton, NJ, OR San Diego, CA, OR San Francisco, CA. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary This role is responsible for supporting Clinical Operations' management objectives to perform clinical trials that are of high quality, and that are delivered to agreed timelines and budget. This role manages clinical operations processes including project planning, budget, resource management, and contract research organization management. This role serves as a key contact and resource for Clinical Study Managers, CRA's and Clinical Trial Assistants. Responsible for ensuring that clinical studies are carried out and delivered according to GCP and company SOPs. Assists with the creation and implementation of policies. Works cross-functionally to ensure that the teams provide required inputs and receive --- TITLE: Manager, AI Engineering EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States (unspecified) SALARY: $122K-$153K POSTED: 2026-04-29 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8526323002?gh_jid=8526323002 EXCERPT: Manager, AI Engineering Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position can be based in San Diego, CA, San Francisco, CA or Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Manager, AI Engineering plays a key role in advancing Acadia's enterprise AI and analytics capabilities. This role designs, builds, and deploys scalable AI/ML and GenAI solutions that deliver measurable business impact across R&D, Commercial, and Corporate functions. As a core member of the Artificial Intelligence organization, the Manager will contribute to the enterprise AI strategy, support responsible AI governance, and help operationalize advanced analytics and machine learning at scale across Acadia globally. Primary Responsibilities - Design, develop, validate, and deploy machine learning, statistical, and GenAI solutions that address complex business problems and support enterprise priorities - Contribute to execution of the --- TITLE: Director, Commercial Sourcing & Procurement EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States (unspecified) SALARY: $178K-$223K POSTED: 2026-05-27 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8560046002?gh_jid=8560046002 EXCERPT: Director, Commercial Sourcing & Procurement Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: San Diego, CA ; San Francisco, CA ; Princeton, NJ Position Summary: The Director, Commercial Sourcing and Procurement will be a strategic leader of the Acadia Sourcing & Procurement team, leading the development of SG&A(Commercial, IT, Professional services, Legal, Contingent Workforce) sourcing strategies for key vendors in North America. This position will play a vital role to ensure Acadia has access to top quality services, technologies, and vendor partners required to support company's growth. It leads the identification, assessment, selection, negotiation, execution of contracts and relationship with key SG&A vendors, and will contribute to the corporate sourcing & procurement policy, vendor management and governance framework and process. This role will be based in San Diego, CA, San Francisco, CA, or Princeton, NJ Primary Duties and Responsibilities: - Develop both immediate and long-term sourcing strategies/plans --- TITLE: Director Clinical Pharmacology EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States (unspecified) SALARY: $199K-$249K POSTED: 2026-02-05 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8384979002?gh_jid=8384979002 EXCERPT: Director Clinical Pharmacology Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position can be based in San Diego, CA OR San Francisco, CA OR Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Director of Clinical Pharmacology will bring deep expertise across both preclinical and clinical development, with a strong track record of success in advancing drug candidates through early development. This individual will serve as a key representative of the Clinical Pharmacology function on cross-functional Asset Teams and will be responsible for leading early-stage programs. Core responsibilities include the strategic planning and execution of Phase 1 clinical trials, including First-in-Human (FIH) and proof-of-concept (PoC) studies in healthy volunteers. This role supports drug development across multiple therapeutic areas, with a focus on neuroscience. Primary Responsibilities - Interpret nonclinical data and translate findings into --- TITLE: Neuroscience Sales Specialist, Lafayette, LA EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Louisiana - Remote (remote) SALARY: $92K-$115K POSTED: 2026-05-22 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8561966002?gh_jid=8561966002 EXCERPT: Neuroscience Sales Specialist, Lafayette, LA Louisiana - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Lafayette, LA Position Summary The Neuroscience Sales Specialist is responsible for achieving sales goals within the assigned territory by building strong customer relationships, delivering compliant and compelling product education, and driving appropriate patient access. This role requires expertise in neuroscience, deep knowledge of the local healthcare landscape, and the ability to partner effectively with healthcare professionals (HCPs) and key stakeholders to deliver meaningful value and service. Primary Responsibilities - Promote Acadia products to HCPs in person and virtually, providing clinical, disease state, and reimbursement information in a compliant and customer-focused manner. - Develop and execute a territory business plan to meet or exceed sales objectives, leveraging market data, customer insights, and quarterly action plans. - Establish and maintain strong relationships with HCPs, including key opinion leaders, advocacy organizations, and other healthcare stakeholders. - Address customer questions, concerns, and objections using advanced dialogue and selling skills. - Tailor --- TITLE: (Senior) Director Clinical Research EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $240K-$300K POSTED: 2026-02-26 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8435950002?gh_jid=8435950002 EXCERPT: (Senior) Director Clinical Research Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Princeton, NJ, San Diego, CA Position Summary The (Senior) Director, Clinical Research will be a highly qualified and motivated individual who will have a leadership role in the development of Acadia programs for rare diseases and/or neurologic and neuropsychiatric disorders. This person will have extensive clinical and scientific knowledge and a strong network in the medical community, and successful experience in leading clinical programs. Primary Responsibilities - Create and execute global clinical development plans consistent with the Company's strategic vision and mission. - Ensure the optimal planning, implementation and interpretation of clinical studies, including synopsis/protocol development, medical monitoring, data analysis and writing of final reports. - Maintain and build productive relationships with investigators, thought leaders and centers of excellence across the scientific community, as well as with colleagues across the Acadia organization. - Interact frequently with sites to support study awareness, --- TITLE: Manager, Commercial Analytics & Insights - Neuro EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States (unspecified) SALARY: $110K-$137K POSTED: 2026-02-03 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8381939002?gh_jid=8381939002 EXCERPT: Manager, Commercial Analytics & Insights - Neuro Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position can be based in San Diego, CA OR San Francisco, CA OR Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary Acadia is seeking a commercially oriented analytics professional to join our Commercial Insights & Performance team. This role focuses on translating complex healthcare data into clear, actionable insights that shape brand strategy and business decisions. This role will partner closely with marketing, sales, and patient value access teams to identify opportunities, diagnose performance drivers, and inform key initiatives. This position requires strong business acumen, fluency in healthcare data sources, and the ability to communicate the “so what” behind the data. This is an individual contributor role focused on execution and analysis, supporting senior team members and business --- TITLE: Director, Global Commercial Product Strategy EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: San Diego, California, United States; South San Francisco, California, United States (unspecified) SALARY: $196K-$245K POSTED: 2026-06-02 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8575181002?gh_jid=8575181002 EXCERPT: Director, Global Commercial Product Strategy San Diego, California, United States; South San Francisco, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position is based in San Diego, CA or San Francisco, CA. Acadia's hybrid model requires this role to work in our office three days per week on average. The Director, Global Commercial Product Strategy is responsible for shaping the commercial product strategy across the product lifecycle, from early development through launch and lifecycle optimization. Leads the cross functional Global Commercialization Team to develop the strategy and strategic plan for product commercialization across markets, inclusive of scenario planning, forecasting, and lifecycle planning. Serves as the commercial voice within the cross-functional Asset Strategy Team, ensuring pipeline assets are positioned for maximum value creation through data-driven insights, robust market understanding, and competitive differentiation. Primary Responsibilities: - Lead end-to-end commercial strategic planning, inclusive of scenario planning, for assigned pipeline asset/s, through early development to launch readiness and commercialization. - Develop target market --- TITLE: Associate Director, Regulatory Affairs Project Planning & Coordination EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States (unspecified) SALARY: $154K-$193K POSTED: 2026-05-20 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8555087002?gh_jid=8555087002 EXCERPT: Associate Director, Regulatory Affairs Project Planning & Coordination Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position can be based in San Diego, CA, San Francisco, CA or Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Associate Director, Regulatory Affairs Project Planning & Coordination is responsible for developing, implementing, and monitoring project plans and best practices that facilitate how the Global Regulatory Affairs department executes its strategic and functional goals. This role will create best practices that maximize the efficiency and impact in which Global Regulatory Affairs develops, endorses, and executes regulatory strategy. This role will also be involved in planning of regulatory submission timelines, compliance and maintenance activities, and department conduct. Primary Responsibilities - Develop and maintain integrated regulatory project plans for global submissions, health authority interactions, and key regulatory activities --- TITLE: Sr. Manager, Chemical Development EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $154K-$193K POSTED: 2026-04-21 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8504889002?gh_jid=8504889002 EXCERPT: Sr. Manager, Chemical Development Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position can be based in Princeton, NJ OR San Diego, CA. Acadia's hybrid model requires this role to work in our office an average of 3 days per week. Position Summary: Responsible for the chemical process development, implementation and management of robust, cost effective, and safe processes for the manufacture of APIs from the research stage, through clinical development and marketing approval. Will be responsible for the technical development, support, innovative solutions and commercialization of drug substances using an external network of providers. This position is integral to the advancement of Acadia's growing portfolio of drug candidates, and will provide technical oversight, expertise and guidance of externalized drug substance development related activities. Primary Responsibilities: - Lead scientific strategy for drug substance development, ensuring scalable, efficient, and compliant processes that meet clinical and commercial needs - Oversee contract service providers (CSPs) --- TITLE: Associate Director, Business Development EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $158K-$198K POSTED: 2026-01-06 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8359293002?gh_jid=8359293002 EXCERPT: Associate Director, Business Development Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Princeton, NJ : San Diego, CA Position Summary: The Associate Director, Business Development will work collaboratively with a variety of company functions including External Innovation (Acadia's R&D Search and Evaluation team), Commercial, and Finance as well as external resources to review, landscape, identify and evaluate external assets to support and enhance the Acadia portfolio. We are seeking an individual with strong analytical and evaluation skills including data gathering and analysis, financial modeling experience and related analysis, competitive intelligence and scientific/commercial analysis of companies and programs in the pharmaceutical and biotech industry, as well as experience with BD transactions. The person in this role must have experience in identifying and analyzing the value of companies and programs within the pharmaceutical industry, building a business case for potential BD opportunities, and working with Executive management to implement corporate Business Development (BD) strategies. Primary --- TITLE: Manager Cybersecurity EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $113K-$142K POSTED: 2026-05-26 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8557168002?gh_jid=8557168002 EXCERPT: Manager Cybersecurity Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Position Summary The Cybersecurity Manager is responsible for supporting Acadia's day‑to‑day cybersecurity operations. This role actively monitors enterprise security tools, investigates alerts, and coordinates incident response activities with internal teams and third‑party security partners. The role supports the development, implementation, and continuous improvement of Acadia's cybersecurity operations, with a strong emphasis on automation and the use of artificial intelligence (AI) to enhance detection, response, and operational efficiency. This Cybersecurity Manager owns Acadia's vulnerability and exposure management programs and leads penetration testing, threat intelligence, threat hunting, and proactive risk identification efforts. Additionally, this role will partner with enterprise stakeholders to support organization‑wide AI and machine learning initiatives, ensuring the confidentiality, integrity, and availability of AI systems. This role helps align cybersecurity practices with business objectives, regulatory requirements, and emerging risks associated with AI technologies. Primary Responsibilities - Actively monitor and manage security tools and service providers to --- TITLE: Sr. IT Service Desk Analyst EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: San Diego, California, United States (unspecified) SALARY: Not disclosed POSTED: 2026-05-27 K401_MATCH: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8557574002?gh_jid=8557574002 EXCERPT: Sr. IT Service Desk Analyst San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Position Summary The Sr. IT Service Desk Analyst is primarily responsible for providing advanced technical support to Acadia Pharmaceutical Executive Leadership while contributing to the effective day-to-day operations of the help and service desk environment. This role actively participates in resolving complex issues and delivering high-quality support to clients across office locations, home offices, offsite facilities, and within our mobile workforce As a Sr. IT Service Desk Analyst, the individual is responsible for but not limited to: performing root cause analysis (RCA), supporting the team's ability to meet service level agreements (SLAs), analyzing queue trends and key performance indicators (KPIs), and providing production and meeting support as needed. The role includes handling escalations, contributing to and assisting with IT projects such as system engineering initiatives and the adoption of emerging technologies, including automation and AI-driven support tools. Additionally, the Senior IT Support Analyst develops, improves, and maintains documentation, --- TITLE: Sr. Health Systems Manager - Texas EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Texas - Remote (remote) SALARY: $158K-$197K POSTED: 2026-04-29 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8530204002?gh_jid=8530204002 EXCERPT: Sr. Health Systems Manager - Texas Texas - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Join Acadia as a Health Systems Manager/Senior Manager and become a key driver of meaningful change in patient care. In this strategic role, you'll build and nurture relationships with leading healthcare institutions-including Centers of Excellence, hospitals, and influential thought leaders-within your region. Your mission: to identify collaborative opportunities that improve access to innovative treatments and expand Acadia's impact in the healthcare landscape. If you're passionate about making a difference and thrive in a dynamic, purpose-driven environment, this is your opportunity to help shape the future of care. Key Responsibilities: - Identify business opportunities, develop complex approaches to account engagement, and execute against Acadia's strategic imperatives. - Identify, develop and advance relationships with influential & relevant Key Medical Experts. - Strong understanding of patient journey and gaps in care to effectively educate on potential EHR interventions within Centers of Excellence and IDN's. - Effectively implement the medication transitions of care --- TITLE: Senior Manager, Packaging and Serialization EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $129K-$161K POSTED: 2026-03-03 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8438214002?gh_jid=8438214002 EXCERPT: Senior Manager, Packaging and Serialization Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Princeton, NJ; San Diego, CA Position Summary: Responsible for coordination of packaging (package design), artwork, and serialization with commercial Drug Product Contract Manufacturing organizations (CMO's), and other third party suppliers for products as identified. Subject matter expert in the field of serialization to oversee our CMOs running commercial and Acadia data management and integration. Experienced in the technical aspects of product introduction into the EU and other global markets as related to serialization, package design, and local requirements. Primary Responsibilities: - Develops and maintains good working relationships with both internal stakeholders and contract manufacturers. - Acquires and maintains scientific and technological knowledge and background of existing and new pharmaceutical (surface) serialization technologies to ensure our CMOs are aligned. Verifies CMO serialization technologies and ensures compliance with pharmaceutical regulatory requirements (EU FMD and DSCSA). - Coordinate periodic CMO Manufacturing meetings preparing --- TITLE: Director, Direct Material and Manufacturing, Sourcing and Procurement EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $178K-$223K POSTED: 2026-06-01 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8571011002?gh_jid=8571011002 EXCERPT: Director, Direct Material and Manufacturing, Sourcing and Procurement Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Position Summary: The Director, Direct Material and Manufacturing, Sourcing and Procurement will be a strategic leader of the Acadia Sourcing & Procurement team, leading the development of all commercial manufacturing and raw materials sourcing category strategies globally. This position will play a vital role to ensure Acadia has access to top quality services, technologies, and vendor partners required to support company's growth. It leads the identification, assessment, selection, negotiation, execution of contracts and relationship with key TDOQ vendors, and will contribute to the corporate sourcing & procurement policy, vendor management and governance framework and process. This role will be based in San Diego, CA or Princeton, NJ Primary Duties and Responsibilities: - Develop global sourcing strategies/plans for vendors in commercial supply chain, packaging and logistics, drug substance, drug formulation, quality assurance, analytical development - Proactively work with business stakeholders including --- TITLE: Associate Director, Quality Operations EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $145K-$181K POSTED: 2026-05-28 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8559878002?gh_jid=8559878002 EXCERPT: Associate Director, Quality Operations Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position is based in San Diego, CA or Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Associate Director, Quality Operations plays a critical role in ensuring the quality, compliance, and integrity of Acadia's clinical and commercial products. This role provides GMP quality oversight for both internal operations and Contract Manufacturing Organizations (CMOs) across all stages of the product lifecycle. The position partners closely with manufacturing and development teams to support reliable supply, regulatory compliance, and continuous improvement in alignment with FDA and global GMP requirements. Primary Responsibilities - Provide GMP quality oversight for internal operations and CMOs supporting clinical and commercial products - Manage batch review, disposition, and release activities for drug substance and drug product manufacturing and packaging - Lead QA oversight of technology transfer, --- TITLE: Senior Director, Patient Support Service Operations & Solutions EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $227K-$284K POSTED: 2026-06-08 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8582707002?gh_jid=8582707002 EXCERPT: Senior Director, Patient Support Service Operations & Solutions Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position is based in either San Diego, CA, or Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Sr. Director, Patient Support Services Operations & Solutions is a critical enterprise leader responsible for architecting, optimizing, and governing the operational backbone of Patient Support Services (PSS). This role oversees HUB operations, specialty pharmacy collaboration, affordability programs, technology enablement, and vendor governance to ensure a seamless, compliant, and high‑quality patient access experience. This leader owns the end‑to‑end patient journey - spanning onboarding, benefits verification, prior authorization, affordability, fulfillment, and ongoing support. The Sr. Director partners closely with PSS Field Leadership, Commercial, Market Access, Trade, IT, Compliance, and Data/Analytics to drive operational excellence, accountability, and continuous improvement that enhances speed‑to‑therapy, access outcomes, and program quality. Primary Responsibilities: PSS --- TITLE: Patient Access Manager - Nashville, TN EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Tennessee - Remote (remote) SALARY: $128K-$160K POSTED: 2026-06-11 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8585560002?gh_jid=8585560002 EXCERPT: Patient Access Manager - Nashville, TN Tennessee - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Nashville, TN; Jackson, TN; Chattanooga, TN Position Summary: The Patient Access Manager (PAM) will provide expert field-based access and reimbursement support, serving as a dedicated point of contact to healthcare providers (HCPs) for their on-label access-related questions regarding company products. This field-based role acts as a critical liaison among HCPs, Specialty Pharmacies (SPs), payers, patients, hub services, and internal cross-functional teams. As a coverage and access subject matter expert, the PAM is integral to ensure patients have timely access to treatment by providing support for customers in an assigned geographic territory. This role requires frequent travel to support the access needs of key stakeholders. PAM is a non-promotional role within ACADIA and adheres to all ACADIA-approved compliance guidelines, including the role-specific Rules of Engagement. Key Responsibilities: - Proactively educate healthcare providers on navigating programs, processes, and access-related requirements to facilitate patient access to ACADIA products via --- TITLE: Technology, AI and Automation Intern, Europe EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Zug, Switzerland (unspecified) SALARY: Not disclosed POSTED: 2026-02-27 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8442634002?gh_jid=8442634002 EXCERPT: Technology, AI and Automation Intern, Europe Zug, Switzerland About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. The Technology, AI & Automation Intern will support Acadia Europe by contributing hands-on technical expertise to identify, prototype, and deliver technology-enabled improvements across the European organization. This internship is planned for a duration of 2-4 months and is intended to provide targeted, project-based support outside of the standard intern program framework. The role is designed to bring current external perspectives on AI and automation into Acadia Europe, while enabling the intern to gain structured exposure to the pharmaceutical business. The intern will contribute cross-functionally to understanding business processes and deliver tangible, value-adding outputs aligned with Acadia's ways of working and compliance requirements. The position is paid and based in Baar (ZG), Switzerland. We are only able to consider students enrolled at Swiss learning institutions with valid work/stay permits. This internship provides hands-on exposure to applying AI and automation in a real-world pharmaceutical setting. The intern will gain insight into cross-functional --- TITLE: Sr. Manager, Government Affairs & Policy EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: San Diego, California, United States (unspecified) SALARY: $149K-$186K POSTED: 2026-04-27 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8512785002?gh_jid=8512785002 EXCERPT: Sr. Manager, Government Affairs & Policy San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position can be based in San Diego, CA, Princeton, NJ or San Francisco, CA. Acadia's hybrid model requires this role to work in our office on average three days per week. Position Summary As the Sr. Manager, Government Affairs & Policy, you will lead compelling internal and external communications that elevate Acadia's policy and advocacy priorities while amplifying our voice with key stakeholders. You will play a meaningful role in supporting state government affairs initiatives, partnering closely with the Director of State Government Affairs & Policy and building relationships that drive real-world policy impact. This opportunity is ideal for a strategic, passionate communicator who thrives at the intersection of healthcare policy, advocacy, and cross‑functional collaboration. Primary Responsibilities - Develop materials to support GAP internal communications and external advocacy programs. These may include internal newsletters, intranet content, program updates, talking points, slide decks; and --- TITLE: Director, Field Force Effectiveness - Rare Franchise EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $194K-$242K POSTED: 2026-05-13 K401_MATCH: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8545783002?gh_jid=8545783002 EXCERPT: Director, Field Force Effectiveness - Rare Franchise Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position is based in San Diego, CA or Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary: As the Director, Field Force Effectiveness for the US Rare Disease franchise you will be responsible for leading efforts and your team to implement and administer initiatives and support services that are critical to maximizing the effectiveness of our field based teams by working in partnership with leadership, Sales, Marketing, and Patient Service groups. This includes ensuring that the field teams are optimally deployed with the correct territory alignment, they are targeting the right customers with the right call plan, they are providing the right level of services to optimize the patient on-boarding journey, they have the right incentive compensation bonus plan that properly rewards/motivating their performance, and --- TITLE: Director Drug Safety & Pharmacovigilance Medical Safety EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States (unspecified) SALARY: $221K-$276K POSTED: 2026-04-23 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8515535002?gh_jid=8515535002 EXCERPT: Director Drug Safety & Pharmacovigilance Medical Safety Princeton, New Jersey, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Director of Drug Safety & Pharmacovigilance is a medical safety expert within the Drug Safety & Pharmacovigilance (PV) function, reporting to the Executive Director of Medical Safety. This role serves as the primary medical safety resource for assigned products across the Acadia portfolio, providing hands-on medical evaluation of safety data, signal detection and assessment, and clinical oversight of pharmacovigilance activities throughout the product lifecycle. The Director contributes product-level medical input to cross-functional safety governance, collaborates with the Executive Director of Medical Safety on complex or escalated safety issues, and supports regulatory submissions and health authority interactions for assigned products. Primary Responsibilities - Serves as the primary medical safety resource for assigned Acadia products, providing product-level clinical --- TITLE: Director, R&D Sourcing and Procurement EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $178K-$223K POSTED: 2026-05-27 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8558441002?gh_jid=8558441002 EXCERPT: Director, R&D Sourcing and Procurement Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Princeton, NJ ; San Diego, CA Position Summary: The Director, R&D Sourcing and Procurement will be a strategic leader of the Acadia Sourcing & Procurement team, leading the development of R&D(Clin Ops, Med Affairs, Translation Meds, Pharmacovigilance, Regulatory Affairs)sourcing strategies for key global vendors This position will play a vital role to ensure Acadia has access to top quality services, technologies, and vendor partners required to support company's growth. It leads the identification, assessment, selection, negotiation, execution of contracts and relationship with key R&D vendors, and will contribute to the corporate sourcing & procurement policy, R&D vendor management and governance framework and SOPs. This role will be based in San Diego, CA, or Princeton, NJ. Primary Duties and Responsibilities: - Develop both immediate and long-term sourcing strategies/plans for the R&D vendors with the focus on clinical operations vendors - Proactively --- TITLE: Senior Associate R&D Quality and Risk Management EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States (unspecified) SALARY: $32.21-$40.29/hr POSTED: 2026-06-11 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8584254002?gh_jid=8584254002 EXCERPT: Senior Associate R&D Quality and Risk Management Princeton, New Jersey, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position can be based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary: This role will work closely with the other team members in Quality Risk & Compliance (QRC) to assist in assessment, reporting on compliance and improvement of processes, tools and systems for Acadia clinical trials' execution in a Good Clinical Practices (GCP) regulated environment. Additional areas of support include Good Pharmacovigilance Practices (GvP), and Good Laboratory Practices (GLP). Involvement in process improvement projects with Subject Matter Experts (SMEs) of multiple functions in clinical research and other departments, is often part of daily activities. This position requires great timekeeping skills, interpersonal collaboration and a great level of independence to carry out assigned tasks. Primary Responsibilities: - Independently calculate, track, QC, and report assigned Key Quality Indicator (KQI) metrics --- TITLE: Manager, Data Analytics & Investigations EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $108K-$136K POSTED: 2026-04-24 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8523018002?gh_jid=8523018002 EXCERPT: Manager, Data Analytics & Investigations Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position is based in Princeton, NJ or San Diego, CA. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary: As the Manager, Data Analytics & Investigations, you will play a highly visible role in strengthening Acadia's healthcare compliance program by leveraging data analytics, audits, and monitoring to proactively identify and mitigate risk. You will collaborate closely with cross‑functional partners across Compliance, Legal, Finance, and Commercial teams to ensure regulatory requirements, internal policies, and ethical standards are consistently upheld. This is an exciting opportunity for a compliance professional who enjoys turning complex data into actionable insights and making a meaningful impact on a growing organization's integrity and culture. Primary Responsibilities: Data Analytics & Reporting - Lead and mature the organization's healthcare compliance data analytics and monitoring program, ensuring scalability, sustainability, --- TITLE: Neuroscience Sales Specialist - Southern New Jersey, NJ EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: New Jersey - Remote (remote) SALARY: $92K-$115K POSTED: 2026-05-19 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8554820002?gh_jid=8554820002 EXCERPT: Neuroscience Sales Specialist - Southern New Jersey, NJ New Jersey - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Philadelphia, NJ Position Summary The Neuroscience Sales Specialist is responsible for achieving sales goals within the assigned territory by building strong customer relationships, delivering compliant and compelling product education, and driving appropriate patient access. This role requires expertise in neuroscience, deep knowledge of the local healthcare landscape, and the ability to partner effectively with healthcare professionals (HCPs) and key stakeholders to deliver meaningful value and service. Primary Responsibilities - Promote Acadia products to HCPs in person and virtually, providing clinical, disease state, and reimbursement information in a compliant and customer-focused manner. - Develop and execute a territory business plan to meet or exceed sales objectives, leveraging market data, customer insights, and quarterly action plans. - Establish and maintain strong relationships with HCPs, including key opinion leaders, advocacy organizations, and other healthcare stakeholders. - Address customer questions, concerns, and objections using advanced dialogue and --- TITLE: Director, Manufacturing EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $173K-$216K POSTED: 2026-04-06 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8488385002?gh_jid=8488385002 EXCERPT: Director, Manufacturing Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Princeton, NJ ; San Diego, CA Position Summary: Responsible for business lead and coordination of commercial Drug Product Contract Manufacturing Organizations (CMO's), and other third-party suppliers for products as identified. Responsible for tracking of ongoing manufacturing schedules to ensure commercial supply levels are maintained and inventory targets are met. Responsible for technical and business evaluation of manufacturing network. Primary Responsibilities: - Team and Project Leadership, capable of leading manufacturing activities and coordinating activities across a matrix team. A SME in DP manufacturing, knowledgeable in development, quality, and regulatory requirements for manufacturing. - Manage all aspects of DP Manufacturing from authoring and revision of manufacturing documents (MBRs, Protocols, QRAs, etc), oversight of manufacturing operation, managing deviations, investigations, and relevant change actions, supporting product release, and ensuring the finished product arrives in warehouse for distribution. - Responsible for DP vendor selection process for new commercial --- TITLE: Neuroscience Sales Specialist - Allentown, PA EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Pennsylvania - Remote (remote) SALARY: $92K-$115K POSTED: 2026-06-09 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8583072002?gh_jid=8583072002 EXCERPT: Neuroscience Sales Specialist - Allentown, PA Pennsylvania - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Allentown, PA Position Summary The Neuroscience Sales Specialist is responsible for achieving sales goals within the assigned territory by building strong customer relationships, delivering compliant and compelling product education, and driving appropriate patient access. This role requires expertise in neuroscience, deep knowledge of the local healthcare landscape, and the ability to partner effectively with healthcare professionals (HCPs) and key stakeholders to deliver meaningful value and service. Primary Responsibilities - Promote Acadia products to HCPs in person and virtually, providing clinical, disease state, and reimbursement information in a compliant and customer-focused manner. - Develop and execute a territory business plan to meet or exceed sales objectives, leveraging market data, customer insights, and quarterly action plans. - Establish and maintain strong relationships with HCPs, including key opinion leaders, advocacy organizations, and other healthcare stakeholders. - Address customer questions, concerns, and objections using advanced dialogue and selling skills. - --- TITLE: Medical Science Liaison / Sr Medical Science Liaison (North Central) EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Idaho - Remote; Iowa - Remote; Minnesota - Remote; Montana - Remote; Nebraska - Remote; Nevada - Remote; North Dakota - Remote; South Dakota - Remote; Utah - Remote (remote) SALARY: $143K-$179K POSTED: 2026-05-06 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8534486002?gh_jid=8534486002 EXCERPT: Medical Science Liaison / Sr Medical Science Liaison (North Central) Idaho - Remote; Iowa - Remote; Minnesota - Remote; Montana - Remote; Nebraska - Remote; Nevada - Remote; North Dakota - Remote; South Dakota - Remote; Utah - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking Talent Near: Minneapolis, MN; Saint Paul, MN; Fargo, ND; Sioux Falls, SD; Omaha, NE; Billings, MT; Boise, ID Position Summary The Medical Science Liaison / Senior Medical Science Liaison plays a pivotal role in advancing Acadia's scientific leadership within a designated therapeutic area. Serving as a trusted scientific partner, this role builds meaningful, long-term relationships with national and regional healthcare professionals to support education on current and emerging Acadia therapies. The MSL / Sr MSL ensures timely, accurate, and impactful medical and scientific exchange that empowers informed clinical decision-making. Through strong collaboration and insight-driven engagement, this position directly contributes to the success of Medical Affairs objectives across the assigned geography. Primary Responsibilities - Build and sustain strong relationships --- TITLE: Long-Term Care Sales Specialist - Miami, FL EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Florida - Remote (remote) SALARY: $92K-$115K POSTED: 2026-06-08 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8580912002?gh_jid=8580912002 EXCERPT: Long-Term Care Sales Specialist - Miami, FL Florida - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Miami, FL Position Summary Responsible for driving sales, developing business, and addressing customer needs within an assigned long-term care (LTC) territory. Manages relationships with prescribers, pharmacists, facility decision-makers, and other members of the LTC care team to ensure appropriate patients are identified, started, and maintained on therapy. Primary Responsibilities - Build and maintain strong relationships with all members of the LTC resident care team, including physicians, physician-extenders (NP/PA), consultant pharmacists, dispensing pharmacists, and nursing facility leadership/staff. - Promote Acadia products by delivering compliant clinical, disease state, and reimbursement education tailored to customer needs. - Identify and address customer questions, concerns, and objections with advanced selling skills. - Develop deep knowledge of customers, practices, and local/regional market trends; apply this insight to business planning. - Create and execute quarterly territory business/action plans, leveraging data to maximize reach, frequency, and impact within budget. - Provide guidance on --- TITLE: Medical Science Liaison / Senior Medical Science Liasion, Florida EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Florida - Remote (remote) SALARY: $143K-$179K POSTED: 2026-06-09 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8575022002?gh_jid=8575022002 EXCERPT: Medical Science Liaison / Senior Medical Science Liasion, Florida Florida - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Position Summary Join Acadia as a Medical Science Liaison / Senior Medical Science Liaison (MSL) and play a critical role in advancing scientific exchange and supporting innovative therapies within a designated therapeutic area. In this field-based role, you will build and maintain trusted relationships with key opinion leaders (KOLs), investigators, and healthcare professionals (HCPs), ensuring access to accurate, up-to-date medical and scientific information. You will serve as a strategic partner to internal teams while contributing valuable field insights that shape medical and development strategies. Primary Responsibilities - Build and maintain relationships with national and regional KOLs, HCPs, patient advocacy groups, and centers of excellence aligned to Medical Affairs strategy - Lead scientific exchange with thought leaders, including discussions on research, clinical data, and emerging therapies - Support clinical trial sites and facilitate investigator-initiated research (IIR) proposals - Maintain deep expertise in therapeutic area, disease state, and --- TITLE: Associate Director R&D AI Solutions & Analytics EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States (unspecified) SALARY: $156K-$196K POSTED: 2026-06-09 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8575535002?gh_jid=8575535002 EXCERPT: Associate Director R&D AI Solutions & Analytics Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position can be based in San Diego, CA, San Francisco, CA, or Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Associate Director, R&D AI Solutions & Analytics will serve as a strategic and technical leader responsible for advancing AI-enabled analytics and digital innovation capabilities across Research & Development (R&D). This role will focus on leading the design, implementation, scaling, and adoption of analytics and AI-driven solutions that improve decision-making, optimize clinical development operations, and enhance portfolio insights across the organization. The individual will partner closely with R&D stakeholders, Digital/IT teams, and external vendors to deliver scalable analytics products, intelligent workflows, AI-enabled solutions, and operational insights capabilities. This role requires a highly collaborative and execution-oriented leader who thrives --- TITLE: Long-Term Care Sales Specialist - Orlando N, FL EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Florida - Remote (remote) SALARY: $92K-$115K POSTED: 2026-05-27 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8565870002?gh_jid=8565870002 EXCERPT: Long-Term Care Sales Specialist - Orlando N, FL Florida - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Orlando, FL Position Summary Responsible for driving sales, developing business, and addressing customer needs within an assigned long-term care (LTC) territory. Manages relationships with prescribers, pharmacists, facility decision-makers, and other members of the LTC care team to ensure appropriate patients are identified, started, and maintained on therapy. Primary Responsibilities - Build and maintain strong relationships with all members of the LTC resident care team, including physicians, physician-extenders (NP/PA), consultant pharmacists, dispensing pharmacists, and nursing facility leadership/staff. - Promote Acadia products by delivering compliant clinical, disease state, and reimbursement education tailored to customer needs. - Identify and address customer questions, concerns, and objections with advanced selling skills. - Develop deep knowledge of customers, practices, and local/regional market trends; apply this insight to business planning. - Create and execute quarterly territory business/action plans, leveraging data to maximize reach, frequency, and impact within budget. - Provide guidance --- TITLE: Senior Manager, Clinical Trial Materials EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Netherlands - Remote (remote) SALARY: Not disclosed POSTED: 2026-04-29 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8521314002?gh_jid=8521314002 EXCERPT: Senior Manager, Clinical Trial Materials Netherlands - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Position Summary: In support of clinical development programs, the Senior Manager of Clinical Trial Materials role oversees Clinical Trial Material (CTM) planning and execution activities, supporting Phase 1-IV and IIS trials. Includes demand forecasting, determination of an appropriate presentation, setting production schedules, protocol review, ensures label compliance with applicable regulations, establishes optimal packaging & distribution strategies, tracks and reconciles drug supplies and monitors product re-test dates. Interface with internal departments and contract research organizations (CROs) as necessary to coordinate the execution of these activities. Implements and ensures group compliance to procedures for the production and distribution of investigation product. Mentor junior colleagues in the CTM team as required. Primary Responsibilities: - Review and Interpretation of a clinical protocol or study overview: - Review and provide feedback during the development of the clinical protocol. - Calculate total demand and translation of total demand into a demand forecast. - Interface with Project --- TITLE: Senior Manager R&D Learning & Development EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) SALARY: $140K-$174K POSTED: 2026-04-09 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8499602002?gh_jid=8499602002 EXCERPT: Senior Manager R&D Learning & Development Princeton, New Jersey, United States; San Diego, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Princeton, NJ ; San Diego, CA Position Summary The Senior Manager R&D Learning & Development supports the development, implementation, and ongoing management of onboarding, training strategies, systems training, and learning processes that build scientific, operational, and future‑ready capabilities across the Research and Development organization and pipeline. Primary Responsibilities - Assist in the design, implementation, and continuous improvement of a tiered onboarding and capability-building curriculum aligned to the evolving needs of the R&D pipeline, including discovery, early development, and late-stage programs. - Utilize experiential learning best practices to effectively engage adult learners and ensure the successful transfer of knowledge. - Support the management of GxP, congress, and data training with internal stakeholders. - Collaborate cross-functionally with R&D subject matter experts to develop disease area, modality, platform, and pipeline-focused training, including investigational asset education and emerging science. - Lead and support --- TITLE: Neuroscience Sales Specialist - San Jose, CA EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: California - Remote (remote) SALARY: $124K-$155K POSTED: 2025-12-15 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8339288002?gh_jid=8339288002 EXCERPT: Neuroscience Sales Specialist - San Jose, CA California - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: San Jose, CA; Palo Alto, CA; Redwood Ctiy, CA; Santa Cruz, CA; Salinas, CA; Marina, CA Position Summary The Neuroscience Sales Specialist is responsible for achieving sales goals within the assigned territory by building strong customer relationships, delivering compliant and compelling product education, and driving appropriate patient access. This role requires expertise in neuroscience, deep knowledge of the local healthcare landscape, and the ability to partner effectively with healthcare professionals (HCPs) and key stakeholders to deliver meaningful value and service. Primary Responsibilities - Promote Acadia products to HCPs in person and virtually, providing clinical, disease state, and reimbursement information in a compliant and customer-focused manner. - Develop and execute a territory business plan to meet or exceed sales objectives, leveraging market data, customer insights, and quarterly action plans. - Establish and maintain strong relationships with HCPs, including key opinion leaders, advocacy organizations, and other healthcare --- TITLE: Long-Term Care Sales Specialist, Milwaukee, Wisconsin EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Illinois - Remote; Iowa - Remote; Wisconsin - Remote (remote) SALARY: $92K-$115K POSTED: 2026-06-01 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8571365002?gh_jid=8571365002 EXCERPT: Long-Term Care Sales Specialist, Milwaukee, Wisconsin Illinois - Remote; Iowa - Remote; Wisconsin - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Milwaukee, WI; Appleton, WI; Waukesha, WI; Dubuque, IA; Rockford, IL As a LTC Sales Specialist, you'll own a defined LTC territory and be the strategic force behind expanding business, identifying opportunities, and delivering solutions that meet the unique needs of facilities and care teams. You'll build trusted relationships with prescribers, pharmacists, administrators, and other key decision‑makers-guiding them in identifying appropriate patients, initiating therapy, and supporting long‑term treatment success. Primary Responsibilities: - Build and maintain strong relationships with all members of the LTC resident care team, including physicians, physician-extenders (NP/PA), consultant pharmacists, dispensing pharmacists, and nursing facility leadership/staff. - Promote Acadia products by delivering compliant clinical, disease state, and reimbursement education tailored to customer needs. - Identify and address customer questions, concerns, and objections with advanced selling skills. - Develop deep knowledge of customers, practices, and local/regional market trends; apply this --- TITLE: Executive Long-Term Care Sales Specialist, North Carolina EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: North Carolina - Remote (remote) SALARY: $124K-$155K POSTED: 2026-02-26 K401_MATCH: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8436712002?gh_jid=8436712002 EXCERPT: Executive Long-Term Care Sales Specialist, North Carolina North Carolina - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Raleigh, NC Responsible for driving sales, developing business, and addressing customer needs within an assigned long-term care (LTC) territory. Manages relationships with prescribers, pharmacists, facility decision-makers, and other members of the LTC care team to ensure appropriate patients are identified, started, and maintained on therapy. Primary Responsibilities - Build and maintain strong relationships with all members of the LTC resident care team, including physicians, physician-extenders (NP/PA), consultant pharmacists, dispensing pharmacists, and nursing facility leadership/staff. - Promote Acadia products by delivering compliant clinical, disease state, and reimbursement education tailored to customer needs. - Identify and address customer questions, concerns, and objections with advanced selling skills. - Develop deep knowledge of customers, practices, and local/regional market trends; apply this insight to business planning. - Create and execute quarterly territory business/action plans, leveraging data to maximize reach, frequency, and impact within budget. - Provide guidance on pricing, --- TITLE: Sr. Manager, R&D AI Solutions & Analytics EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States (unspecified) SALARY: $134K-$167K POSTED: 2026-05-28 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8557166002?gh_jid=8557166002 EXCERPT: Sr. Manager, R&D AI Solutions & Analytics Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position can be based in San Diego, CA, Princeton, NJ or San Francisco, CA. Acadia's hybrid model requires this role to work in our office on average three days per week. Position Summary The Sr. Manager, R&D AI Solutions & Analytics plays a critical role in advancing AI‑enabled analytics and digital innovation across Research & Development. This role focuses on designing, developing, and scaling analytics and AI solutions that strengthen decision‑making, optimize clinical development operations, and deliver actionable portfolio insights. As a hands‑on contributor within an innovation‑driven team, this individual partners closely with R&D leaders, Digital/IT teams, and external vendors to deliver scalable analytics products, dashboards, intelligent workflows, and AI‑enabled capabilities that create measurable business impact. Primary Responsibilities - Design and deliver analytics and AI‑enabled solutions supporting Clinical Development, Clinical Operations, --- TITLE: Long-Term Care Sales Specialist - Central Michigan EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Michigan - Remote (remote) SALARY: $92K-$115K POSTED: 2026-05-22 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8561968002?gh_jid=8561968002 EXCERPT: Long-Term Care Sales Specialist - Central Michigan Michigan - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Lansing, MI; South Bend, IN Position Summary Responsible for driving sales, developing business, and addressing customer needs within an assigned long-term care (LTC) territory. Manages relationships with prescribers, pharmacists, facility decision-makers, and other members of the LTC care team to ensure appropriate patients are identified, started, and maintained on therapy. Primary Responsibilities - Build and maintain strong relationships with all members of the LTC resident care team, including physicians, physician-extenders (NP/PA), consultant pharmacists, dispensing pharmacists, and nursing facility leadership/staff. - Promote Acadia products by delivering compliant clinical, disease state, and reimbursement education tailored to customer needs. - Identify and address customer questions, concerns, and objections with advanced selling skills. - Develop deep knowledge of customers, practices, and local/regional market trends; apply this insight to business planning. - Create and execute quarterly territory business/action plans, leveraging data to maximize reach, frequency, and impact within budget. - --- TITLE: Director, Clinical Trial Materials EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States (unspecified) SALARY: $183K-$229K POSTED: 2026-04-02 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8481650002?gh_jid=8481650002 EXCERPT: Director, Clinical Trial Materials Princeton, New Jersey, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Princeton, NJ Position Summary: In support of clinical development programs, the Director of Clinical Trial Materials role oversees Clinical Trial Material (CTM) planning and execution activities, supporting Phase 1-IV and IIS trials. Includes demand forecasting, determination of an appropriate presentation, setting production schedules, protocol review, ensures label compliance with applicable regulations, establishes optimal packaging & distribution strategies, tracks and reconciles drug supplies and monitors product re-test dates. Interface with internal departments and contract research organizations (CROs) as necessary to coordinate the execution of these activities. Implements and ensures group compliance to procedures for the production and distribution of investigation product. Manage junior colleagues in the CTM team as required. Primary Responsibilities: - Review and Interpretation of a clinical protocol or study overview: - Review and provide feedback during the development of the clinical protocol. - Calculate total demand and translation of total demand into a demand --- TITLE: Long-Term Care Sales Specialist, Sarasota, FL EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Florida - Remote (remote) SALARY: $92K-$115K POSTED: 2026-05-22 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8562063002?gh_jid=8562063002 EXCERPT: Long-Term Care Sales Specialist, Sarasota, FL Florida - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Sarasota, FL Position Summary Responsible for driving sales, developing business, and addressing customer needs within an assigned long-term care (LTC) territory. Manages relationships with prescribers, pharmacists, facility decision-makers, and other members of the LTC care team to ensure appropriate patients are identified, started, and maintained on therapy. Primary Responsibilities - Build and maintain strong relationships with all members of the LTC resident care team, including physicians, physician-extenders (NP/PA), consultant pharmacists, dispensing pharmacists, and nursing facility leadership/staff. - Promote Acadia products by delivering compliant clinical, disease state, and reimbursement education tailored to customer needs. - Identify and address customer questions, concerns, and objections with advanced selling skills. - Develop deep knowledge of customers, practices, and local/regional market trends; apply this insight to business planning. - Create and execute quarterly territory business/action plans, leveraging data to maximize reach, frequency, and impact within budget. - Provide guidance on pricing, --- TITLE: Associate Director, AI/ML Engineering EMPLOYER: Acadia Pharmaceuticals Inc LOCATION: Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States (unspecified) SALARY: $159K-$199K POSTED: 2026-06-02 K401_MATCH: yes (not source-backed) MENTAL_HEALTH_SUPPORT: yes (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://acadia.com/en-us/careers/job-board/8565787002?gh_jid=8565787002 EXCERPT: Associate Director, AI/ML Engineering Princeton, New Jersey, United States; San Diego, California, United States; South San Francisco, California, United States About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Please note that this position is based in San Diego, CA, South San Francisco, CA, or Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Associate Director, AI/ML Engineering serves as a hands-on technical leader driving the design, architecture, and delivery of Generative AI and agentic AI solutions across the enterprise. This role builds scalable multi-agent systems, connects AI solutions to enterprise data and tools, and ensures safe, reliable deployment through robust evaluation and guardrail frameworks. The position also applies strong machine learning and foundation model expertise to deliver high-impact use cases within a regulated biopharmaceutical environment. Primary Responsibilities - Design, build, and deploy agentic AI workflows that automate and transform complex business processes, leveraging multi-agent orchestration frameworks (e.g., LangGraph, AutoGen, CrewAI, or equivalent). - --- TITLE: Senior Casualty Claims Specialist EMPLOYER: W. R. Berkley Corporation LOCATION: Westbrook, ME, US (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 K401_MATCH: yes (not source-backed) APPLY_URL: https://careers-berkley.icims.com/jobs/13814/senior-casualty-claims-specialist/job EXCERPT: Senior Casualty Claims Specialist Westbrook, ME, US Company Details Acadia Insurance is a regional property casualty insurer with offices throughout the Northeast. As a member of W.R. Berkley Corporation (NYSE: WRB), one of the largest property casualty insurance holding companies in the United States, our financial strength and integrity are two of the main reasons why Independent Agents place business with us. Acadia is rated A+ (Superior) by A.M. Best, with an A+ claim paying ability rating by Standard & Poor's. At Acadia, we value our employees, our customers and our communities. Employees at Acadia are part of a progressive company where everyone can make a difference. We promote an inclusive environment which encourages continuous learning and the chance to grow and develop. Company URL: https://www.acadiainsurance.com/ Responsibilities Investigate, evaluate and resolve assigned high exposure claims in accordance with company standards, procedures, and state regulatory requirements. Perform investigations in a timely and thorough manner to ensure accurate decisions on coverage, liability, and damage issues affecting claim resolutions. Effectively negotiate with insureds and third parties, listening carefully to their demands and using an objective approach to resolve the claim fairly. Control file-related expenses through efficient utilization and monitoring of "outside" vendors. Inform other departments of positive/negative conditions noted during investigations which may impact company results. Manage existing workload --- TITLE: Loss Control Consultant EMPLOYER: W. R. Berkley Corporation LOCATION: Marlborough, MA, US (unspecified) SALARY: $110K-$120K POSTED: 2026-06-12 K401_MATCH: yes (not source-backed) APPLY_URL: https://careers-berkley.icims.com/jobs/14111/loss-control-consultant/job EXCERPT: Loss Control Consultant Marlborough, MA, US Company Details Acadia Insurance is a regional property casualty insurer with offices throughout the Northeast. As a member of W.R. Berkley Corporation (NYSE: WRB), one of the largest property casualty insurance holding companies in the United States, our financial strength and integrity are two of the main reasons why Independent Agents place business with us. Acadia is rated A+ (Superior) by A.M. Best, with an A+ claim paying ability rating by Standard & Poor's. At Acadia, we value our employees, our customers and our communities. Employees at Acadia are part of a progressive company where everyone can make a difference. We promote an inclusive environment which encourages continuous learning and the chance to grow and develop. Company URL: https://www.acadiainsurance.com/ Responsibilities Loss Control Consultant Conducts surveys and services accounts by identifying and evaluating hazards and controls pertaining to all lines of coverage. Develops client-related service plans based on needs analysis and assists the client with problem resolution, policy and procedure development and solution implementation. Services existing accounts according to mutually agreed upon plans developed for each account. Participates in client training and education. Submits recommendations to improve conditions which will mitigate or control the hazards identified and follows-up on recommendations. Assists accounts on potential exposures and promotes the value of Loss Control and sound safety p --- TITLE: Senior Director, Pharmaceutical Strategy and Development Leader EMPLOYER: Crinetics Pharmaceuticals INC LOCATION: San Diego, CA (unspecified) SALARY: $214K-$268K POSTED: 2026-05-12 K401_MATCH: yes (not source-backed) APPLY_URL: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/San-Diego-CA/Senior-Director--Pharmaceutical-Strategy-and-Development-Leader_JR000446 EXCERPT: Senior Director, Pharmaceutical Strategy and Development Leader San Diego, CA Crinetics is a pharmaceutical company based in San Diego, California that develops much-needed therapies for people with rare endocrine diseases. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and robust pipeline across preclinical and clinical development. We are driven by science with a patient-centric and team-oriented culture. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Come join our team as we transform the lives of others. Position Summary: The Senior Director, Pharmaceutical Development Team Leader (PDTL) is responsible for developing and leading the execution of comprehensive, compound-specific Technical Operations strategies to meet the global project team's (GPT) needs. This role provides leadership to interdisciplinary teams, managing multiple assets through various stages of development, and collaborates with various functional areas to achieve optimal development and business results. Essential Job Functions and Responsibilities: These may include but are not limited to: Develop, refine, update, and oversee Technical Operations project plans from multiple inputs, with emphasis on the alignment of these plans with strategic objectives, the decomposition of major objectives into discrete WBS-level work packages, the mapping of internal and cross-functional interdependencies, and the management of project risks. Perform detailed --- TITLE: Medical Science Liaison, Hematology Oncology, Quebec Atlantic EMPLOYER: AbbVie Inc. LOCATION: Remote | Montreal, QC, Canada (remote) SALARY: Not disclosed POSTED: 2026-06-12 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013581716-medical-science-liaison-hematology-oncology-quebec-atlantic EXCERPT: Medical Science Liaison, Hematology Oncology, Quebec Atlantic Remote | Montreal, QC, Canada Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Recruitment Fraud Alert AbbVie has become aware of fraudulent recruitment-related phishing attempts. We encourage all candidates to remain vigilant and exercise caution when responding to messages regarding employment opportunities. AbbVie in Canada recruiters will only communicate with candidates using an official @abbvie.com email address or a verified LinkedIn account. Joining AbbVie means you will be part of a team of outstanding professionals dedicated to making a remarkable impact on patients' lives. At AbbVie, we conduct ground-breaking science on a global scale every day. AbbVie Canada is one of the Best Workplaces in Canada. When choosing your career path, choose to be remarkable. AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, vision care, virology, women's health , and gastroenterology, in addition to products and services --- TITLE: Senior Scientist II - Biologics Drug Product Development EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-12 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013581601-senior-scientist-ii-biologics-drug-product-development EXCERPT: Senior Scientist II - Biologics Drug Product Development North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie's R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy). AbbVie is seeking a highly motivated candidate for the position of Senior Scientist II, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics drug product formulation development, predictive stability, in-use, and quality risk management (QRM) . This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers. Key Responsibilities: Lead matrix drug product teams for one or more internal and external projects and represent Bio --- TITLE: Associate Director, Field Analytics - Oncology Franchise A & E EMPLOYER: AbbVie Inc. LOCATION: Florham Park, NJ, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013069731-associate-director-field-analytics-oncology-franchise-a-e EXCERPT: Associate Director, Field Analytics - Oncology Franchise A & E Florham Park, NJ, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Associate Director, Field Planning, Oncology is responsible for leading call planning and targeting efforts, directing sales force structure and sizing initiatives, managing territory alignments, as well as executing analyses that enable the Oncology demand generating and facilitating teams to be more effective and efficient. The individual will partner with peer analytic and technology functions as well as the Oncology commercial teams to ensure that field teams are deployed and supported in line with the respective brands' strategy. Function Responsibilities Include: Strategic Planning : Play a key role in partnering with commercial leadership to proactively align on long range strategic plans for the Oncology brands, identifying and responding to business needs as they arise. Infuse a customer-focused mindset to deliver business solutions to ensure field deployment efforts are aligned with, and in support of, strategic imperatives. Targeting : Partner with Marketing, Sales, Field Planning & Analytics Team (FPAT), and Marketing Analytics & Business --- TITLE: Pharmaceutical Production Lead - All Shifts EMPLOYER: Medline Inc. LOCATION: Waukegan, Illinois (unspecified) SALARY: Not disclosed POSTED: 2026-05-14 K401_MATCH: yes (not source-backed) APPLY_URL: https://medline.wd5.myworkdayjobs.com/Medline/job/Waukegan-Illinois/Pharmaceutical-Production-Lead---All-Shifts_R2605412 EXCERPT: Pharmaceutical Production Lead - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago --- TITLE: Senior Medical Director, Oncology Clinical Development EMPLOYER: AbbVie Inc. LOCATION: Florham Park, NJ, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013517246-senior-medical-director-oncology-clinical-development EXCERPT: Senior Medical Director, Oncology Clinical Development Florham Park, NJ, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: Oversees the direction, planning, execution, and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy. Responsibilities: Manages the design and implementation of one or more clinical development programs in support of an overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. Oversees project-related education of investigators, study site personnel, and AbbVie study staff. Has overall responsibility for oversight of clinical studies, monitoring overall study integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for oversight of study enrollment and overall timelines for key deliverables. Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on --- TITLE: Pharmaceutical Manufacturer Relations Executive EMPLOYER: Humana Inc. LOCATION: Remote Nationwide (remote) SALARY: Not disclosed POSTED: 2026-06-10 K401_MATCH: yes (not source-backed) APPLY_URL: https://humana.wd5.myworkdayjobs.com/CenterWell_External_Career_Site/job/Remote-Nationwide/Pharmaceutical-Manufacturer-Relations-Executive_R-419074 EXCERPT: Pharmaceutical Manufacturer Relations Executive Remote Nationwide posted: Posted 2 Days Ago --- TITLE: Director, Market Access & Policy - Canada EMPLOYER: Biocryst Pharmaceuticals INC LOCATION: 4 Locations (unspecified) SALARY: Not disclosed POSTED: 2026-06-04 K401_MATCH: yes (not source-backed) APPLY_URL: https://biocryst.wd501.myworkdayjobs.com/External/job/US_North-Carolina_Remote/Market-Access-Director---Canada_JR100142 EXCERPT: Director, Market Access & Policy - Canada 4 Locations COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. ESSENTIAL DUTIES & RESPONSIBILITIES: Develop and implement national and provincial market access and stakeholder engagement strategies to ensure optimal policy conditions and reimbursement for current and future BioCryst products. Lead development and submission of HTA dossiers to bodies such as CDA and INESSS. Effectively navigate the pCPA environment; lead negotiations with pCPA and provinces to secure PLAs. Lead development of all provincial healthcare payer and private payer reimbursement files; lead negotiations of PLAs with public and private payers. Support the development and implementation of annual plans for public and private payer customers in Canada. Manage all public and private payer and policy related issues. Lead all required annual reporting, incl. PMPRB, provincial/territorial payers, private payers. Ensure compliance with PMPRB (Patented Medicine Prices Review Board) --- TITLE: Pharmaceutical Product Operator - All Shifts EMPLOYER: Medline Inc. LOCATION: Waukegan, Illinois (unspecified) SALARY: Not disclosed POSTED: 2026-05-14 K401_MATCH: yes (not source-backed) APPLY_URL: https://medline.wd5.myworkdayjobs.com/Medline/job/Waukegan-Illinois/Pharmaceutical-Product-Operator_R2605410 EXCERPT: Pharmaceutical Product Operator - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago --- TITLE: Senior Scientist II / Principal Scientist I, Biologics Drug Product Development EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013490176-senior-scientist-ii-principal-scientist-i-biologics-drug-product-development EXCERPT: Senior Scientist II / Principal Scientist I, Biologics Drug Product Development North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Description: Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie's R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy). AbbVie is seeking a highly motivated candidate for the position of Senior Scientist II / Principal Scientist I, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics drug product formulation and process development, scale-up and tech transfer. This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers. Key Responsibilities: Represent Bio DPD in the cross-functional Product Presentation and Device Strategy --- TITLE: Pharmaceutical Production Technician - All Shifts EMPLOYER: Medline Inc. LOCATION: Waukegan, Illinois (unspecified) SALARY: Not disclosed POSTED: 2026-05-14 K401_MATCH: yes (not source-backed) APPLY_URL: https://medline.wd5.myworkdayjobs.com/Medline/job/Waukegan-Illinois/Pharmaceutical-Production-Technician---All-Shifts_R2605411 EXCERPT: Pharmaceutical Production Technician - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago --- TITLE: Director, Oncology Market Access Strategy EMPLOYER: AbbVie Inc. LOCATION: Mettawa, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990012924586-director-oncology-market-access-strategy EXCERPT: Director, Oncology Market Access Strategy Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: AbbVie is looking for a Director of Oncology Market Access Strategy. This position is responsible for market access marketing leadership for Emrelis (telisotuzumab vedotin), an antibody-drug conjugate approved for second-line, c-Met expressing non-squamous non-small cell lung cancer (NSCLC) accompanied by a companion diagnostic for patient selection. Emrelis represents AbbVie's first oncology solid tumor launch, a key strategic priority for the enterprise, and is in dynamic growth mode. The Marketing Director will develop strategy and tactics across all payer channels (e.g. Commercial, Medicare, Medicaid, VA, etc). Lead strategic alignment with the Emrelis Integrated Brand Team, developing Market Access strategies with stakeholders in the Oncology commercial organization and US Medical Affairs. As the first AbbVie-led solid tumor and biomarker driven launch in oncology, the Director will bring relevant launch expertise and articulate strategy. The Director will leverage data, analytics and strong strategic mind-set in all aspects of running the marketing component of the business. Throughout their work, the director will provide --- TITLE: Pharmaceutical Information Specialist EMPLOYER: Merck & Co., Inc. LOCATION: CHN - Shanghai - Shanghai (Tower A) (unspecified) SALARY: Not disclosed POSTED: 2026-06-05 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Tower-A/Pharmaceutical-Information-Specialist_R401276-1 EXCERPT: Pharmaceutical Information Specialist CHN - Shanghai - Shanghai (Tower A) posted: Posted 7 Days Ago --- TITLE: Medical Director Pharmacovigilance EMPLOYER: Apogee Therapeutics Inc LOCATION: Remote (remote) SALARY: $285K-$330K POSTED: 2026-06-01 K401_MATCH: yes (not source-backed) APPLY_URL: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5151650007 EXCERPT: Medical Director Pharmacovigilance Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Medical Director, Pharmacovigilance to join the Apogee Clinical Development team. In this --- TITLE: Pharmaceutical Information Manager EMPLOYER: Merck & Co., Inc. LOCATION: CHN - Shanghai - Shanghai (Trading) (unspecified) SALARY: Not disclosed POSTED: 2026-06-04 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Trading/Pharmaceutical-Information-Manager_R401755-2 EXCERPT: Pharmaceutical Information Manager CHN - Shanghai - Shanghai (Trading) posted: Posted 8 Days Ago --- TITLE: Marketing Manager II - Consumer - Oncology EMPLOYER: AbbVie Inc. LOCATION: Mettawa, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013095581-marketing-manager-ii-consumer-oncology EXCERPT: Marketing Manager II - Consumer - Oncology Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Marketing Manager I/II - DTC Patient Marketing will be a key driver of Elahere® (mirvetuximab soravtansine-gynx) direct-to-consumer and patient-facing marketing strategies. Elahere is the first FDA-approved ADC for FRα-positive, platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer - representing a transformative therapy for a patient population with significant unmet need. This role is responsible for developing, executing, and optimizing patient-directed promotional programs and multichannel campaigns that meaningfully connect women living with platinum-resistant ovarian cancer to information about Elahere and FRα testing. The MMI/II will serve as a critical connector between patient insights, brand strategy, HCP marketing, and media execution - bringing the patient voice to the forefront of the Elahere brand. Key Responsibilities Patient Marketing Strategy & Campaign Execution Develop and execute integrated, multichannel DTC patient marketing plans in alignment with overall Elahere brand strategy, ensuring consistency across paid media, owned channels, digital platforms, and patient support programs. Lead development of patient-facing promotional materials including --- TITLE: Pharmaceutical Information Specialist,AI EMPLOYER: Merck & Co., Inc. LOCATION: CHN - Shanghai - Shanghai (Tower A) (unspecified) SALARY: Not disclosed POSTED: 2026-06-05 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Tower-A/Pharmaceutical-Information-Specialist-AI_R400237-1 EXCERPT: Pharmaceutical Information Specialist,AI CHN - Shanghai - Shanghai (Tower A) posted: Posted 7 Days Ago --- TITLE: Director, Pharmaceutical Analytical Sciences EMPLOYER: Merck & Co., Inc. LOCATION: USA - New Jersey - Rahway (unspecified) SALARY: Not disclosed POSTED: 2026-05-14 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/USA---New-Jersey---Rahway/Director--Pharmaceutical-Analytical-Sciences_R396510-1 EXCERPT: Director, Pharmaceutical Analytical Sciences USA - New Jersey - Rahway posted: Posted 29 Days Ago --- TITLE: Principal Scientist I, Biologics Analytical R&D (External Programs) EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013110371-principal-scientist-i-biologics-analytical-r-d-external-programs- EXCERPT: Principal Scientist I, Biologics Analytical R&D (External Programs) North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Overview: AbbVie Biologics Analytical Research & Development (Biologics ARD) is a global analytical sciences organization responsible for CMC analytical activities related to the development of AbbVie's therapeutic biologic products. Our scope includes AbbVie's diverse pipeline of innovative therapeutic biologics medicines, including monoclonal antibodies, antibody drug conjugates (ADC), and other novel modalities, and spans from the selection of Discovery candidate molecules through the transition of analytical methods and testing to operations partners for late stage development. We are building a world-class team of scientists and leaders who will drive the advancement of industry-leading analytical capabilities and make meaningful contributions to advance AbbVie's pipeline of innovative medicines. Careers in AbbVie Biologics ARD provide unique opportunities to work with global and cross-functional teams to drive exceptional science and innovative product development strategies. The Analytical Development - External Programs group within Biologics ARD is responsible for early development (through clinical proof of concept) of programs with outsourced analytical activities. --- TITLE: Sr. Pharmaceutical Info Specialist,AI EMPLOYER: Merck & Co., Inc. LOCATION: CHN - Jiangsu - Suzhou (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Jiangsu---Suzhou/Sr-Pharmaceutical-Info-Specialist-AI_R393894-2 EXCERPT: Sr. Pharmaceutical Info Specialist,AI CHN - Jiangsu - Suzhou posted: Posted 30+ Days Ago --- TITLE: Sr. Pharmaceutical Info Specialist, Onco EMPLOYER: Merck & Co., Inc. LOCATION: CHN - Shandong - Yantai (unspecified) SALARY: Not disclosed POSTED: 2026-06-01 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shandong---Yantai/Sr-Pharmaceutical-Info-Specialist--Onco_R398232-1 EXCERPT: Sr. Pharmaceutical Info Specialist, Onco CHN - Shandong - Yantai posted: Posted 11 Days Ago --- TITLE: Associate Director, Strategic Engagement (Thought Leader Liaison), Mid-Atlantic EMPLOYER: Mirum Pharmaceuticals Inc LOCATION: US Remote (remote) SALARY: Not disclosed POSTED: 2026-05-27 APPLY_URL: https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5145629007 EXCERPT: Associate Director, Strategic Engagement (Thought Leader Liaison), Mid-Atlantic US Remote MISSION Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we're looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously. POSITION SUMMARY The Associate Director, Strategic Engagement also known as Thought Leader Liaison (TLL) serves as a key strategic partner between Mirum Pharmaceuticals and the healthcare community, focusing on cultivating and maintaining relationships with key opinion leaders (KOLs), thought leaders, and other external stakeholders. This role is responsible for building scientific credibility, supporting brand strategy, and ensuring aligned, compliant engagement with external experts to enhance awareness and education. Area of focus will largely be supporting the Hepatology and Gastroenterology community supporting our existing and future products in Alagille, PFIC, PBC, PSC and Hepatitis D. States likely to be included in territory include: PA, DE, VA, MD, DC, WV, OH, KY, MI JOB FUNCTIONS/RESPONSIBILITIES - Develop and communicate the strategic vision and operational plan for engaging KOLs. - Develop and oversee development and execution of individual KOL Mapping KOLs plans. - Partner closely with the Director, Marketing - KOL Strategy and Congress Planning to ensure alignment. - Build and maintain productive, collaborative, and compliant relationships with peers leading teams in Marketing, Market Access, Patient Services, and Medical Affairs. - Work --- TITLE: Manager, Product Quality EMPLOYER: AbbVie Inc. LOCATION: Irvine, CA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013497107-manager-product-quality EXCERPT: Manager, Product Quality Irvine, CA, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: Responsible for quality of assigned products which may include small molecule pharmaceuticals and/or biologics products, combination products, and medical devices to ensure business objectives are met with regards to on time delivery of product while assuring compliance to local, divisional, and corporate policies and external agency regulations worldwide. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), Intermediates or Drug Products produced by AbbVie plants or by third-party manufacturers, In Licensing relationships, or Co-Marketing relationships. Develops in concert with Regulatory Affairs, the appropriate regulatory strategies for product brands. Grade is commensurate on level of overall responsibility. Responsibilities Maintains the primary quality lead with management oversight for project activities and the team members (within and outside of AbbVie) to achieve on-time quality deliverables, high customer value, and profitable results. Primary driver for the quality and compliance aspects of product transfers and organization optimization. Participates in the development of global Product Quality Assurance strategy to support pharmaceuticals, biologics, --- TITLE: Sr. Pharmaceutical Info Specialist EMPLOYER: Merck & Co., Inc. LOCATION: CHN - Shanghai - Shanghai (Tower A) (unspecified) SALARY: Not disclosed POSTED: 2026-05-21 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Tower-A/Sr-Pharmaceutical-Info-Specialist_R399628 EXCERPT: Sr. Pharmaceutical Info Specialist CHN - Shanghai - Shanghai (Tower A) posted: Posted 22 Days Ago --- TITLE: Asso. Pharmaceutical Information Manager, Onco EMPLOYER: Merck & Co., Inc. LOCATION: CHN - Guangdong - Foshan (unspecified) SALARY: Not disclosed POSTED: 2026-05-28 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Guangdong---Foshan/Asso-Pharmaceutical-Information-Manager--Onco_R400857-1 EXCERPT: Asso. Pharmaceutical Information Manager, Onco CHN - Guangdong - Foshan posted: Posted 15 Days Ago --- TITLE: Associate Director, Commercial Strategy and Insights EMPLOYER: Maplight Therapeutics Inc LOCATION: Burlington, MA (unspecified) SALARY: $195K-$220K POSTED: 2026-05-22 K401_MATCH: yes (not source-backed) APPLY_URL: https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5228687008 EXCERPT: Associate Director, Commercial Strategy and Insights Burlington, MA Who We Are: MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms. What You'll Do: We are seeking a highly motivated Associate Director, Commercial Strategy and Insights to support the development and execution of commercial initiatives across our growing organization. This role will help build market research, forecasting, and competitive intelligence that inform launch planning, market opportunity assessments, and commercial strategy for our lead asset and broader pipeline. As the commercial function grows, the role is expected to evolve into a role on our Insights and Analytics team. The Associate Director will work closely with Commercial Leadership, Marketing, Market Access, Medical Affairs, Sales, Finance, Business Development, and Clinical teams to inform data-driven strategies that maximize product value and support long-term company growth. The ideal candidate combines analytical rigor, strategic thinking, and strong cross-functional collaboration within a fast-paced pre-commercial biotech environment. Responsibilities : - Support market research, forecasting and analytics workstreams that inform integrated commercial strategies for our lead asset and pipeline products. - Conduct market assessments, competitive analyses, and opportunity evaluations to inform strategic decision-making. - Partner with cross-functional teams to define product positioning, target customer segments, and value propositions. - Support commercial launch planning activities for new products and indications. - Identify commercial risks, opportunities, and mitigation --- TITLE: Senior Director, Trade & Channel Operations EMPLOYER: Amylyx Pharmaceuticals Inc LOCATION: Cambridge, MA (unspecified) SALARY: $255K-$287K POSTED: 2026-04-06 K401_MATCH: yes (not source-backed) APPLY_URL: https://job-boards.greenhouse.io/amylyx/jobs/5843909004 EXCERPT: Senior Director, Trade & Channel Operations Cambridge, MA Amylyx has an audacious mission to usher in a new era for treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitment to the communities we serve. We are a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS). Our mission is powered by our people. Our core values - be audacious, be curious, be authentic, be engaged, and be accountable - creating a culture of caring. Amylyx has assembled an experienced team ready to take action because the communities we serve have no time to wait. If you share our passion and are determined to tackle some of medicine's toughest problems, we encourage you to read the opportunity below and apply. The Opportunity The Senior Director, Trade & Channel Operations will be responsible for building Amylyx's U.S. distribution and channel model from the ground up in preparation for a future commercial launch of our lead product candidate. This individual will architect the distribution strategy, create the operational infrastructure necessary for launch, and partner cross functionally to ensure Amylyx is fully prepared to commercialize with excellence. As a key member of the Market Access team, this role will influence launch readiness, customer service delivery, and ongoing performance across distribution partners. Responsibilities - Design and build Amylyx's U.S. distribution model across specialty pharmacy, specialty distributor, and 3PL channels to support product launch - Lead --- TITLE: Werkstudent (m/w/d) Pharmaceutical Technical Solutions EMPLOYER: Merck & Co., Inc. LOCATION: DEU - Niedersachsen - Friesoythe (unspecified) SALARY: Not disclosed POSTED: 2026-05-12 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/DEU---Niedersachsen---Friesoythe/Werkstudent--m-w-d--Quality-Assurance-Systems_R384362 EXCERPT: Werkstudent (m/w/d) Pharmaceutical Technical Solutions DEU - Niedersachsen - Friesoythe posted: Posted 30+ Days Ago --- TITLE: Senior Vice President, Sales EMPLOYER: Amylyx Pharmaceuticals Inc LOCATION: Flexible/ U.S. Based (unspecified) SALARY: $353K-$397K POSTED: 2026-05-13 K401_MATCH: yes (not source-backed) APPLY_URL: https://job-boards.greenhouse.io/amylyx/jobs/5994725004 EXCERPT: Senior Vice President, Sales Flexible/ U.S. Based Amylyx has an audacious mission to usher in a new era for treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitment to the communities we serve. We are a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS). Our mission is powered by our people. Our core values - be audacious, be curious, be authentic, be engaged, and be accountable - creating a culture of caring. Amylyx has assembled an experienced team ready to take action because the communities we serve have no time to wait. If you share our passion and are determined to tackle some of medicine's toughest problems, we encourage you to read the opportunity below and apply. The Opportunity The SVP of Sales will play a critical leadership role in building and executing the commercial strategy for a pre‑commercial biotechnology company preparing for its first product launch. This individual will be responsible for designing and implementing the Go‑To‑Market (GTM) strategy, recruiting and developing a high‑performing sales organization, establishing strong relationships with Key Opinion Leaders (KOLs), ensuring full sales force readiness ahead of launch and driving performance. We anticipate hiring the Senior Vice President, Sales in September 2026. The ideal candidate combines strategic vision with hands‑on execution experience in specialty pharma or biotech launches and thrives in a fast‑paced, build‑from‑scratch environment. Responsibilities Enterprise Commercial Leadership - Shape overall U.S. commercial --- TITLE: Scientist, Pharmaceutical Analytical Sciences EMPLOYER: Merck & Co., Inc. LOCATION: USA - New Jersey - Rahway (unspecified) SALARY: Not disclosed POSTED: 2026-06-02 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/USA---New-Jersey---Rahway/Scientist--Pharmaceutical-Analytical-Sciences_R395348-2 EXCERPT: Scientist, Pharmaceutical Analytical Sciences USA - New Jersey - Rahway posted: Posted 10 Days Ago --- TITLE: Senior Counsel, Global Commercial Legal - Oncology EMPLOYER: AbbVie Inc. LOCATION: Florham Park, NJ, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013520616-senior-counsel-global-commercial-legal-oncology EXCERPT: Senior Counsel, Global Commercial Legal - Oncology Florham Park, NJ, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The role of Senior Counsel, Global Commercial Legal is responsible for developing legal strategy for AbbVie's Oncology medicines. As a Senior Counsel at AbbVie, you will partner closely with cross-functional teams to shape decisions that bring great possibilities to patients ethically and effectively. This role builds on your foundational legal experience, enabling you to navigate regulatory complexity, assess risk, and influence business outcomes, all while developing leadership capabilities for long-term career growth. A successful candidate will be motivated by the opportunity to address and solve emerging issues with a strategic and creative business-oriented approach and provide expert counsel on decisions impacting our commercial strategies. Key Responsibilities Include: • Serve as a key legal advisor to cross-functional teams within AbbVie's Oncology business unit, providing proactive counsel on commercial, regulatory, or operational issues. Legal advice will be given on topics such as new product/indication launches, patient support models, marketing strategies, promotion, scientific exchange, regulatory submissions and managed healthcare --- TITLE: Sr. Pharmaceutical Info Specialist, ANA EMPLOYER: Merck & Co., Inc. LOCATION: CHN - Shanghai - Shanghai (Tower A) (unspecified) SALARY: Not disclosed POSTED: 2026-06-02 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Tower-A/Sr-Pharmaceutical-Info-Specialist--ANA_R395198-1 EXCERPT: Sr. Pharmaceutical Info Specialist, ANA CHN - Shanghai - Shanghai (Tower A) posted: Posted 10 Days Ago --- TITLE: Pharmacist, Pharmacy Solutions EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013419296-pharmacist-pharmacy-solutions EXCERPT: Pharmacist, Pharmacy Solutions North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The primary role is to function as a licensed pharmacist engaged in the practice of pharmacy. Position is responsible for the daily operations of the pharmacy which includes the preparation, dispensing, and delivery of medications as well as the provision of pharmaceutical care to patients and interaction with health care professionals to assure safe and effective medication therapy. This practice of pharmacy may include but are not limited to: patient counseling; dispensing of drugs; monitoring appropriate drug use; providing drug information; ensuring proper documentation and record keeping for all prescriptions; providing information on therapeutic values, reactions, drug interactions and side effects; supervising licensed pharmacy technicians assisting in the practice of pharmacy; complying with Federal, State, and local pharmacy laws and HIPAA guidelines; carrying out interventions when appropriate, noting recommendations in patient notes. Responsibilities Receive and review prescription orders Review and assess therapy for each patient's prescription to determine therapeutic appropriateness Interact with Patient Care Coordinators, pharmacy technicians, PSPs and other --- TITLE: Pharmaceutical Information Manager, Onco EMPLOYER: Merck & Co., Inc. LOCATION: CHN - Beijing - Beijing (Oriental Towers) (unspecified) SALARY: Not disclosed POSTED: 2026-06-04 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Beijing---Beijing-Oriental-Towers/Pharmaceutical-Information-Manager--Onco_R400628-2 EXCERPT: Pharmaceutical Information Manager, Onco CHN - Beijing - Beijing (Oriental Towers) posted: Posted 8 Days Ago --- TITLE: Principal Scientist I, Biologics Analytical Research and Development EMPLOYER: AbbVie Inc. LOCATION: San Francisco, CA, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-12 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013590896-principal-scientist-i-biologics-analytical-research-and-development EXCERPT: Principal Scientist I, Biologics Analytical Research and Development San Francisco, CA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: About the Team AbbVie Biologics Analytical Research & Development (Biologics ARD) is a global analytical sciences organization responsible for CMC analytical development of AbbVie's pipeline of innovative therapeutic biologic products. We are a world-class team of scientists and leaders united by a shared mission to advance industry-leading analytical capabilities and meaningfully contribute to the advancement of AbbVie's pipeline of innovative medicines. The Biologics ARD team at the AbbVie Bay Area site in South San Francisco has a long and rich history of biologics development. Located in a state-of-the-art facility housing end-to-end CMC development capabilities, the team works collaboratively to advance novel biologic therapeutics - including multi-specifics, ADCs, antibodies, and novel modalities - into first-in-human clinical development and through to clinical proof of concept. Careers in AbbVie Biologics ARD provide unique opportunities to work with cross-functional and global teams to drive exceptional science and innovative product development strategies. Role Summary We are seeking a highly skilled --- TITLE: Asso. Pharmaceutical Information Manager EMPLOYER: Merck & Co., Inc. LOCATION: CHN - Beijing - Beijing (Oriental Towers) (unspecified) SALARY: Not disclosed POSTED: 2026-06-04 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Beijing---Beijing-Oriental-Towers/Asso-Pharmaceutical-Information-Manager_R399328-1 EXCERPT: Asso. Pharmaceutical Information Manager CHN - Beijing - Beijing (Oriental Towers) posted: Posted 8 Days Ago --- TITLE: Pharmaceutical Technician (WDA) EMPLOYER: Merck & Co., Inc. LOCATION: SGP - Singapore - Singapore (70 Tuas West Dr) (unspecified) SALARY: Not disclosed POSTED: 2026-06-11 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/SGP---Singapore---Singapore-70-Tuas-West-Dr/Pharmaceutical-Technician--WDA-_R378025 EXCERPT: Pharmaceutical Technician (WDA) SGP - Singapore - Singapore (70 Tuas West Dr) posted: Posted Yesterday --- TITLE: Director, Oncology Market Access Marketing EMPLOYER: AbbVie Inc. LOCATION: Florham Park, NJ, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013458596--director-oncology-market-access-marketing EXCERPT: Director, Oncology Market Access Marketing Florham Park, NJ, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: AbbVie is looking for a Director of Oncology US Market Access Marketing, ETENTA. This position is responsible for market access marketing leadership for ETENTA (etentamig), a bispecific antibody in development for Multiple Myeloma. ETENTA is in late-stage clinical trials and would represent AbbVie's first launch in Multiple Myeloma, a key strategic priority for the enterprise. The Oncology Market Access Marketing Director for ETENTA will be accountable for market access marketing strategy across all payer channels, including Commercial, Medicare, Medicaid, VA, and other relevant access segments, as well as key account and community oncology channels, as applicable. This role will lead strategic alignment with Market Access field teams and coordinate strategy, communication, and alignment across US Market Access channel and policy partners, the Oncology Commercial Organization, and US Medical Affairs. As the market access marketing subject matter expert for the ETENTA Integrated Brand Team, the Director will develop market access strategies and tactics that support brand objectives and reflect --- TITLE: Pharmaceutical Technician (WDA) EMPLOYER: Merck & Co., Inc. LOCATION: SGP - Singapore - Singapore (70 Tuas West Dr) (unspecified) SALARY: Not disclosed POSTED: 2026-06-02 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/SGP---Singapore---Singapore-70-Tuas-West-Dr/Pharmaceutical-Technician--WDA-_R392851 EXCERPT: Pharmaceutical Technician (WDA) SGP - Singapore - Singapore (70 Tuas West Dr) posted: Posted 10 Days Ago --- TITLE: Associate Scientist II, Drug Metabolism and Distribution EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013523566-associate-scientist-ii-drug-metabolism-and-distribution EXCERPT: Associate Scientist II, Drug Metabolism and Distribution North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: We are seeking an Associate Scientist II to join our Drug Metabolism and Disposition Team within the Quantitative Translation and ADME Sciences organization in Development Sciences at AbbVie Pharmaceuticals. This position is an opportunity to join a dynamic team and work on in vitro and in vivo biotransformation studies. In this role, you will leverage cutting-edge analytical technologies and workflows to solve problems, advance our pipeline and drive pharmaceutical innovation. The ideal candidate will combine strong technical expertise with a desire to learn and grow and create solutions that will accelerate drug discovery and improve patient outcomes. This role will work collaboratively with multiple teams within Discovery, Development Sciences and the Clinical Pharmacology organization to perform analyses and implement technologies to deliver precise, reliable, and reproducible solutions. Communication skills are key to being able to interface with technical and non-technical stakeholders. Responsibilities Perform routine tasks competently and independently and generate reliable and consistent results. Lab based --- TITLE: Operator – Start-up of a New Pharmaceutical Facility EMPLOYER: Merck & Co., Inc. LOCATION: NLD - North Brabant - Boxmeer (unspecified) SALARY: Not disclosed POSTED: 2026-06-03 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/NLD---North-Brabant---Boxmeer/Operator---Nieuwe-Farmaceutische-Fabriek_R393536-1 EXCERPT: Operator – Start-up of a New Pharmaceutical Facility NLD - North Brabant - Boxmeer posted: Posted 9 Days Ago --- TITLE: Senior Scientist I / II - Biologics Analytical R&D EMPLOYER: AbbVie Inc. LOCATION: North Chicago, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013433776-senior-scientist-i-ii-biologics-analytical-r-d EXCERPT: Senior Scientist I / II - Biologics Analytical R&D North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: AbbVie Biologics Analytical Research & Development (Biologics Analytical R&D) is a global analytical sciences organization responsible for all CMC analytical activities related to the development of AbbVie's pharmaceutical products. Our scope includes AbbVie's diverse pipeline of innovative therapeutic biologic medicines and spans from the selection of Discovery candidate molecules through the transition of analytical methods and testing to commercial labs to support product launch. We are building a world-class team of scientists and leaders who will drive the advancement of industry-leading analytical capabilities and make meaningful contributions to advance AbbVie's pipeline of innovative medicines. Careers in AbbVie Biologics Analytical R&D provide unique opportunities to work with global and cross-functional teams to drive exceptional science and innovative product development strategies. The biologics early analytical development group develops state-of-the-art analytical techniques for analysis of therapeutic proteins and other novel biologic molecules using separation science and other biophysical techniques. We are looking for diverse candidates with strong --- TITLE: Sr. Pharmaceutical Info Specialist，Retail EMPLOYER: Merck & Co., Inc. LOCATION: CHN - Xinjiang - Urumuqi (Tianshan District) (unspecified) SALARY: Not disclosed POSTED: 2026-05-13 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Xinjiang---Urumuqi-Tianshan-District/Sr-Pharmaceutical-Info-Specialist-Retail_R398280-1 EXCERPT: Sr. Pharmaceutical Info Specialist，Retail CHN - Xinjiang - Urumuqi (Tianshan District) posted: Posted 30 Days Ago --- TITLE: Director, Marketing - Oncology EMPLOYER: AbbVie Inc. LOCATION: Mettawa, IL, United States (unspecified) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013363906-director-marketing-oncology- EXCERPT: Director, Marketing - Oncology Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: Drives marketing operations for Venclexta 1VEN Operations team. Provides positive leadership and productive influence across and around enterprise. Leverage data, analytics and strategic mind-set in all aspects of running the marketing component of the business. Exhibits P&L mindset. Effectively orchestrate work across internal teams and external partners including agencies, etc. Responsibilities: •Vision and Strategy: Provide overarching leadership and direction for Marketing vision, strategies, plans and resource investment for franchise and/or functional unit. Align and lead the charge. Encompass a “One AbbVie” mindset and perspective in all strategies. •Leadership: Set tone and priorities for scale and scope of accountability. Influence and persuade across multiple external and internal constituents (stakeholders and partners). Lead and develop direct, indirect and cross-business team. Infuse AbbVie Ways of Working and Talent Philosophy in day-to-day leadership and management of the business. Uses coaching effectively and efficiently to create high-performing teams and elevate team's marketing skills and knowledge. •Action and Accountability: Determine appropriate action, execution, tracking and --- TITLE: Représentant(e) en ventes pharmaceutiques / Pharmaceutical Sales Representative EMPLOYER: Merck & Co., Inc. LOCATION: CAN - Quebec - Quebec City (unspecified) SALARY: Not disclosed POSTED: 2026-06-03 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CAN---Quebec---Quebec-City/Reprsentant-e--en-ventes-pharmaceutiques---Pharmaceutical-Sales-Representative_R401727-1 EXCERPT: Représentant(e) en ventes pharmaceutiques / Pharmaceutical Sales Representative CAN - Quebec - Quebec City posted: Posted 9 Days Ago --- TITLE: Senior Operator – Start-up of a New Pharmaceutical Facility EMPLOYER: Merck & Co., Inc. LOCATION: NLD - North Brabant - Boxmeer (unspecified) SALARY: Not disclosed POSTED: 2026-06-03 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/NLD---North-Brabant---Boxmeer/Senior-Operator---Start-up-of-a-New-Pharmaceutical-Facility_R401808 EXCERPT: Senior Operator – Start-up of a New Pharmaceutical Facility NLD - North Brabant - Boxmeer posted: Posted 9 Days Ago --- TITLE: Growth Account Manager EMPLOYER: AcuityMD LOCATION: Boston or Remote (remote) SALARY: $130K-$150K POSTED: 2026-06-07 PARENTAL_LEAVE_WEEKS: 6 (not source-backed) LEARNING_BUDGET_OFFERED: yes (not source-backed) APPLY_URL: https://job-boards.greenhouse.io/acuitymd/jobs/5985736004 EXCERPT: Growth Account Manager Boston or Remote Growth Account Manager AcuityMD is a software and data platform that accelerates access to medical technologies. Each year, the FDA approves ~6,000 new medical devices. Our platform helps MedTech companies get these products to physicians more effectively so they can improve patient care with the latest technology. We're backed by Benchmark, Redpoint, ICONIQ Growth and Ajax Health and we help MedTech companies identify how their products are used, understand why outcomes vary, and identify opportunities where physicians can better serve their patients. We're looking for a results-driven Account Manager to own and grow a portfolio of 50-75 customer accounts with a clear focus on driving ARR growth . Your top priority will be expanding revenue through upsells, renewals, and strategic account management. In this role, you'll deepen customer relationships, identify growth opportunities, and ensure a seamless transition from new business to long-term success. You'll partner closely with Sales and Customer Success, staying aligned on customer goals while keeping pace with product updates and industry trends. If you thrive in a fast-paced SaaS environment and are motivated by hitting and exceeding ARR targets, we'd love to meet you. Team Mission We are building a best-in-class Commercial Team and establishing a repeatable go-to-market motion. We are hiring a team of high caliber Enterprise SaaS sales, marketing, and customer success professionals to thoughtfully engage C-Suite, VPs, General Managers, and other corporate decision makers across the Medical Device Industry. Our Commercial Team takes a proactive, consultative, and high-touch --- TITLE: Associate Scientist II (Contract), Drug Product Analytics EMPLOYER: Vaxcyte Inc LOCATION: San Carlos, California, United States (unspecified) SALARY: $51-$56/hr POSTED: 2026-05-21 K401_MATCH: yes (not source-backed) APPLY_URL: https://boards.greenhouse.io/vaxcyte/jobs/5224522008?gh_jid=5224522008 EXCERPT: Associate Scientist II (Contract), Drug Product Analytics San Carlos, California, United States Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered. *AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary: Vaxcyte is looking for an energetic and talented individual to join our Drug Product Development team. The candidate must have knowledge of and practical experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) using a variety of methods, including immunoassays, chromatography, spectrophotometric techniques, light scattering, and particle sizing. --- TITLE: Improvement Officer - Start-up of a new pharmaceutical facility EMPLOYER: Merck & Co., Inc. LOCATION: NLD - North Brabant - Boxmeer (unspecified) SALARY: Not disclosed POSTED: 2026-06-03 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/NLD---North-Brabant---Boxmeer/Improvement-Officer---Start-up-of-a-new-pharmaceutical-facility_R401802-2 EXCERPT: Improvement Officer - Start-up of a new pharmaceutical facility NLD - North Brabant - Boxmeer posted: Posted 9 Days Ago --- TITLE: Senior Strategic Partnership Account Manager, 12 months EMPLOYER: AbbVie Inc. LOCATION: Remote | Toronto, ON, Canada (remote) SALARY: Not disclosed POSTED: 2026-06-10 PARENTAL_LEAVE_WEEKS: 12 (not source-backed) NON_BIRTH_PARENT_LEAVE_WEEKS: 12 (not source-backed) K401_MATCH: yes (not source-backed) APPLY_URL: https://jobs.smartrecruiters.com/AbbVie/3743990013477039-senior-strategic-partnership-account-manager-12-months- EXCERPT: Senior Strategic Partnership Account Manager, 12 months Remote | Toronto, ON, Canada Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Joining AbbVie means you will be part of a team of outstanding professionals dedicated to making a remarkable impact on patients' lives. At AbbVie, we conduct ground-breaking science on a global scale every day. AbbVie Canada is one of the Best Workplaces in Canada. When choosing your career path, choose to be remarkable. AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, vision care, virology, women's health , and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. We have an opportunity for a Senior Strategic Account Manager to join our Pharmacy Innovation & Trade Strategy team, reporting to the Pharmacy Partnership & Strategy Manager. In this exciting role, you will be responsible for identifying, developing and executing on partnership opportunities with --- TITLE: Pharmaceutical Sales Representative/ Représentant(e) en ventes pharmaceutiques (Alberta) EMPLOYER: Merck & Co., Inc. LOCATION: 3 Locations (unspecified) SALARY: Not disclosed POSTED: 2026-06-08 K401_MATCH: yes (not source-backed) APPLY_URL: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CAN---Quebec---Kirkland-16750-Transcanada/Pharmaceutical-Sales-Representative---Reprsentant-e--en-ventes-pharmaceutiques--Alberta-_R401426-1 EXCERPT: Pharmaceutical Sales Representative/ Représentant(e) en ventes pharmaceutiques (Alberta) 3 Locations posted: Posted 4 Days Ago --- [PASTE YOUR RESUME OR SKILLS HERE]