# FewerJobs export - 100 curated jobs Generated: 2026-08-11T04:24:03.945Z Source: https://fewerjobs.com ## Filters applied - **q**: AcuityMD - **quality_floor**: default - **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 ### Senior Software Engineer, Infrastructure - AcuityMD - Location: Boston or Remote (remote) - Salary: $180K-$250K - Posted: 2026-06-07 - Parental leave: 16 weeks (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acuitymd/jobs/5755363004 - Excerpt: Senior Software Engineer, Infrastructure Boston or Remote Senior Software Engineer, Infrastructure AcuityMD is a software and data platform that accelerates access to medical technologies. We help MedTech companies understand how their products are used, why customers vary, and identify opportunities for physicians to better serve their patients. Each year, the FDA approves ~6,000 new medical devices. Our solution 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. We're a high-growth AI and Data company scaling rapidly. We are a team of agentic builders who rely heavily on AI development practices to accelerate our ability to deliver value to our customers. We believe in extreme ownership and agency, where every engineer takes responsibility for working throughout the organization to land impact with customers. We're a close-knit team that enables high levels of autonomy by constantly communicating our intentions, sharing problems and learnings, and helping each other learn and grow. As an Infrastructure Engineer, you'll be directly interacting with other teams across Engineering and production. Through collaboration, you'll help design, build, and operate the platform primitives-compute, networking, storage, CI/CD, and developer tooling-that power our applications end-to-end. You'll drive reliability, security, and efficiency while enabling a great developer experience. You'll also contribute to our strategic goals as we evolve our infrastructure and our practices to maximize our internal and customer impact. Team Mission Our Platform Team is the backbone that keeps product ### Senior Software Engineer, Applications - AcuityMD - Location: Boston or Remote (remote) - Salary: $190K-$250K - Posted: 2026-06-07 - Parental leave: 16 weeks (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acuitymd/jobs/5991090004 - Excerpt: Senior Software Engineer, Applications Boston or Remote Senior Software Engineer, Applications AcuityMD is a software and data platform that accelerates access to medical technologies. We help MedTech companies understand how their products are used, why customers vary, and identify opportunities for physicians to better serve their patients. Each year, the FDA approves ~6,000 new medical devices. Our solution 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. We're a high-growth AI and Data company scaling rapidly. We are a team of agentic builders who rely heavily on AI development practices to accelerate our ability to deliver value to our customers. We believe in extreme ownership and agency, where every engineer takes responsibility for working throughout the organization to land impact with customers. We're a close-knit team that enables high levels of autonomy by constantly communicating our intentions, sharing problems and learnings, and helping each other learn and grow. We are currently looking for Software Engineers to join our growing Application Teams. In this role, you will have the opportunity to work on all aspects of the current product and future product development. You will work with other passionate engineers on complex projects that help bring cutting-edge technologies to patients. In this role, you will have the opportunity to work on all aspects of the current product and future product development. You will work with other passionate engineers on complex ### Product Marketing Manager - AcuityMD - Location: Boston or Remote (remote) - Salary: $150K-$180K - Posted: 2026-06-07 - Parental leave: 8 weeks (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acuitymd/jobs/5989009004 - Excerpt: Product Marketing Manager Boston or Remote Product Marketing Manager AcuityMD is a technology company that connects software and data to help MedTech companies of all sizes transform how they bring their products to market. Each year, the FDA approves ~6,000 new medical devices. By combining quality data and tailored workflows, our platform helps MedTech commercial teams get their devices into the hands of the healthcare providers who need them to improve patient care. We're backed by Benchmark, Redpoint, and Ajax Health, and we're on a mission to accelerate the adoption of cutting-edge medical technologies. As a Product Marketing Manager, you will be responsible for driving and owning go-to-market strategy inclusive of positioning, messaging, packaging, and pricing for a product surface area within our platform. You will be responsible for understanding how our customers want to buy, and helping them to do so, by articulating customer pain points and our corresponding solutions and value props clearly and in their own language, leading new feature and product launches, and creating assets that support field enablement and customer marketing activity. You will have a deep understanding of the industry, our buyers, and the competitive landscape and will be expected to distill market and competitive insights to inform our positioning and Product Roadmap in collaboration with Product Management. The Product Marketing Manager role is highly visible and cross-functional, requiring regular collaboration with Product Management, Sales, Customer Success, and Marketing among other functions. You should enjoy rolling up your sleeves as a self-starter and moving ### Strategic Account Executive - AcuityMD - Location: Boston or Remote (remote) - Salary: Not disclosed - Posted: 2026-06-07 - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acuitymd/jobs/5722137004 - Excerpt: Strategic Account Executive Boston or Remote Strategic Account Executive AcuityMD is a software and data platform that accelerates access to medical technologies. We help MedTech companies understand how their products are used, why customers vary, and identify opportunities for physicians to better serve their patients. Each year, the FDA approves ~6,000 new medical devices. Our solution 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. We're a high-growth AI and Data company scaling rapidly. As a Strategic Account Executive, you'll play a pivotal role in bringing a category-defining software product to the MedTech market. You will lead efforts to identify and close strategic opportunities at major accounts. This role offers the chance to accelerate your professional growth while working alongside a team of exceptionally smart, driven, and passionate individuals. 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 VPs, General Managers, and other corporate decision-makers across the Medical Device Industry. Our Commercial Team takes a proactive, consultative, and high-touch approach when working with customers, investing heavily in pre-sales through onboarding and training to ensure customers are on the road to success from Day 1. Responsibilities Identify, negotiate, and close opportunities at both existing accounts and new MedTech enterprises. You will establish a vision and plan ### Senior Product Manager - AcuityMD - Location: Boston or Remote (remote) - Salary: $175K-$215K - Posted: 2026-06-07 - Parental leave: 8 weeks (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acuitymd/jobs/5920568004 - Excerpt: Senior Product Manager Boston or Remote Senior Product Manager AcuityMD is a software and data platform that accelerates access to medical technologies. We help MedTech companies understand how their products are used, why customers vary, and identify opportunities for physicians to better serve their patients. Each year, the FDA approves ~6,000 new medical devices. Our solution 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. We're a high-growth AI and Data company scaling rapidly. We're hiring a Senior Product Manager to take ownership of a major product area. You'll work across engineering, design, go-to-market, and customers to solve high-impact problems, build scalable software, and deliver tangible business value. You'll thrive here if you're (1) a high-agency generalist with a strong product management foundation - skilled at cutting through ambiguity, shipping great products, and working in fast-moving, collaborative environments - and (2) AI literate. We value both deep PM craft (e.g., understanding user needs, making smart tradeoffs, and driving outcomes) AND some comfort with getting uncomfortable using the latest AI tools (e.g., prototyping and diving into the code base with the latest models). This is an opportunity to join a high-growth company during a critical scaling phase. You'll be optimizing mature products and shaping what comes next. Team Mission We are building a world-class product team to build software features as meticulously crafted and data driven as the highly specialized ### Customer Success Manager, Growth - AcuityMD - Location: Boston or Remote (remote) - Salary: $120K-$160K - Posted: 2026-06-07 - Parental leave: 8 weeks (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acuitymd/jobs/5779991004 - Excerpt: Customer Success Manager, Growth Boston or Remote Customer Success Manager, Growth 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, 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. Customer Success Managers are trusted advisors to key stakeholders at our accounts, delivering strategic insights to drive their business initiatives. Additionally, this role will be primarily responsible for guiding users and organizations through ongoing platform adoption and value recognition. Customer Success Managers are successful by developing deep and personal relationships with our user base, driving user adoption 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 VPs, General Managers, and other corporate decision makers across the Medical Device Industry. Our Commercial Team takes a proactive, consultative, and high-touch approach when working with customers, investing heavily in pre-sales through onboarding and training to ensure customers are on the road to success from Day 1. We strongly encourage people of all backgrounds to apply. Responsibilities Effectively manage a large book of business across many different account specialties and unique ### Program Manager - AcuityMD - Location: Boston or Remote (remote) - Salary: $190K-$240K - Posted: 2026-06-12 - Parental leave: 8 weeks (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acuitymd/jobs/6019042004 - Excerpt: Program Manager Boston or Remote Program 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, 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. In this role, you will be responsible for ensuring our largest, most strategic accounts have a world-class experience on the AcuityMD platform. These customers represent the most complex organizations, technology portfolios, and technical requirements. They also represent the greatest opportunity for our company to have a positive impact on their businesses and on the world, as they bring diverse and impactful medical technology to the patients in need. The customers that the Program Manager will be responsible for are often in a constant state of implementation, as they deepen their initial adoption of and repeatedly expand their use of AcuityMD to more and more of their business units. You will partner closely with sales executives, solutions engineers, customer success managers in the Enterprise and Strategic segments to ensure a cohesive experience for these critical customers. Team Mission The Professional Services team is part of a tightly integrated commercial organization that is responsible for the end-to-end customer experience from initial sale and implementation through ongoing application support, ### Enterprise Account Executive - AcuityMD - Location: Boston or Remote (remote) - Salary: $240K-$300K - Posted: 2026-06-07 - Parental leave: 8 weeks (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acuitymd/jobs/5722026004 - Excerpt: Enterprise Account Executive Boston or Remote Enterprise Account Executive AcuityMD is a software and data platform that accelerates access to medical technologies. We help MedTech companies understand how their products are used, why customers vary, and identify opportunities for physicians to better serve their patients. Each year, the FDA approves ~6,000 new medical devices. Our solution 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. We're a high-growth AI and Data company scaling rapidly. We are looking for a dynamic and results-oriented Enterprise Account Executive to join our sales team. In this position, you will play a key role in driving revenue growth by identifying and securing new business opportunities, managing the full sales cycle from prospecting to closing, and fostering strong relationships with clients in the MedTech industry. 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 VPs, General Managers, and other corporate decision-makers across the Medical Device Industry. Our Commercial Team takes a proactive, consultative, and high-touch approach when working with customers, investing heavily in pre-sales through onboarding and training to ensure customers are on the road to success from Day 1. Responsibilities Identify, negotiate, and close opportunities at both existing accounts and new MedTech enterprises. Quarterback the enterprise sales motion by conducting ### Senior Data Product Manager - AcuityMD - Location: Boston or Remote (remote) - Salary: $175K-$215K - Posted: 2026-06-07 - Parental leave: 8 weeks (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acuitymd/jobs/5973606004 - Excerpt: Senior Data Product Manager Boston or Remote Senior Data Product Manager AcuityMD is a software and data platform that accelerates access to medical technologies. We help MedTech companies understand how their products are used, why customers vary, and identify opportunities for physicians to better serve their patients. Each year, the FDA approves ~6,000 new medical devices. Our solution 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. We're a high-growth AI and Data company scaling rapidly. As a Senior Data Product Manager, you will build and refine AcuityMD's data assets, products, model and platform. You'll play a critical role in identifying market opportunities, crafting compelling product offerings, and bringing agentic AI solutions to life. You will build empathy for our users, solve complex problems and drive business success for our customers and for AcuityMD. You will report to the Chief Product Officer, and work cross-functionally with engineering and customer-facing teams. Team Mission We are building a world-class data products team to meticulously craft and deliver data assets and algorithms that enable new workflows and power AcuityAI to solve customer problems. Our team is the critical link between what our engineers build and what our customers need. We are looking for product leaders to develop deep empathy for our users, apply data and AI to prioritize user needs, and bring new capabilities to life by aligning and coordinating across technical ### Deal Desk Analyst - AcuityMD - Location: Boston or Remote (remote) - Salary: $100K-$120K - Posted: 2026-06-07 - Parental leave: 8 weeks (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acuitymd/jobs/6001580004 - Excerpt: Deal Desk Analyst Boston or Remote Deal Desk Analyst AcuityMD is a software and data platform that accelerates access to medical technologies. We help MedTech companies understand how their products are used, why customers vary, and identify opportunities for physicians to better serve their patients. Each year, the FDA approves ~6,000 new medical devices. Our solution 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. We're a high-growth AI and Data company scaling rapidly. As a Deal Desk Analyst, you will play a critical role in helping our Commercial organization move quickly while maintaining operational accuracy and compliance. You will partner closely with Account Executives, Legal, Finance, and Customer Success to structure, review, and process deals that support efficient growth. In this role, you'll help ensure our quoting and contracting processes scale effectively, identify operational bottlenecks, and improve the systems and workflows that power our revenue engine. Team Mission Deal Desk exists to increase the velocity of the Commercial organization at AcuityMD and drive excellence across the team through strategy, operations, and analysis. We aim to build and improve processes that enable the Commercial and Revenue teams to scale as efficiently as possible, while providing an outstanding customer experience. We are a highly collaborative group that partners cross-functionally with teams across AcuityMD to drive impact. Responsibilities Support the creation, review, and processing of quotes and order forms within CRM ### Growth Account Manager - AcuityMD - Location: Boston or Remote (remote) - Salary: $130K-$150K - Posted: 2026-06-07 - Parental leave: 6 weeks (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### Engineering Manager, Adoption and Value Realization - AcuityMD - Location: Boston or Remote (remote) - Salary: $220K-$265K - Posted: 2026-06-07 - Parental leave: 8 weeks (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acuitymd/jobs/5821410004 - Excerpt: Engineering Manager, Adoption and Value Realization Boston or Remote Engineering Manager, Adoption and Value Realization AcuityMD is a software and data platform that accelerates access to medical technologies. We help MedTech companies understand how their products are used, why customers vary, and identify opportunities for physicians to better serve their patients. Each year, the FDA approves ~6,000 new medical devices. Our solution 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. We're a high-growth AI and Data company scaling rapidly. We are a team of agentic builders who rely heavily on AI development practices to accelerate our ability to deliver value to our customers. We believe in extreme ownership and agency, where every engineer takes responsibility for working throughout the organization to land impact with customers. We're a close-knit team that enables high levels of autonomy by constantly communicating our intentions, sharing problems and learnings, and helping each other learn and grow. We are looking for a strongly technical and empathetic engineering leader to lead our Adoption and Value Realization team, focused on driving meaningful user engagement with our existing product functionality and ensuring customers realize clear, demonstrable value from AcuityMD. As the founding manager of this new team, you will be instrumental in guiding the team's technical investments, achieving product success, growing the team, and mentoring engineers. You will join the engineering leadership team to help shape the ### Senior Machine Learning Engineer, Data & Intelligence Products - AcuityMD - Location: Boston or Remote (remote) - Salary: Not disclosed - Posted: 2026-06-07 - Parental leave: 8 weeks (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acuitymd/jobs/5986789004 - Excerpt: Senior Machine Learning Engineer, Data & Intelligence Products Boston or Remote Senior Machine Learning Engineer, Data & Intelligence Products AcuityMD is a software and data platform that accelerates access to medical technologies. We help MedTech companies understand how their products are used, why customers vary, and identify opportunities for physicians to better serve their patients. Each year, the FDA approves ~6,000 new medical devices. Our solution 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. We're a high-growth AI and Data company scaling rapidly. We are a team of agentic builders who rely heavily on AI development practices to accelerate our ability to deliver value to our customers. We believe in extreme ownership and agency, where every engineer takes responsibility for working throughout the organization to land impact with customers. We're a close-knit team that enables high levels of autonomy by constantly communicating our intentions, sharing problems and learnings, and helping each other learn and grow. In this role, you will help lead the evolution of AcuityMD's core healthcare data assets by applying statistical and machine learning techniques to convert messy, real-world health data into insight about the healthcare market. You will design and ship predictive models and data products, improve the quality and interpretability of existing models, and deliver high-confidence, repeatable intelligence that fuels our MedTech-specific modules. You will identify new approaches and new data sources that extend ### Acuity Adaptable ICU Nurse - CommonSpirit Health - Location: UNAVAILABLE, UNAVAILABLE, UNAVAILABLE (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - 401(k) match: listed (not source-backed) - Apply: https://careers-commonspirit.icims.com/jobs/471973/acuity-adaptable-icu-nurse/job - Excerpt: Acuity Adaptable ICU Nurse UNAVAILABLE, UNAVAILABLE, UNAVAILABLE Where You'll Work Are you ready to join a healthcare family where your values align with ours? At Dignity Health - Yavapai Regional Medical Center (DH-YRMC), now a proud part of CommonSpirit Health, a not-for-profit integrated healthcare provider, our core mission guides every decision and every interaction. Here, you'll discover more than just a job; you'll find rewarding career opportunities across a comprehensive network of inpatient and outpatient services. From a vibrant community hospital, YRMC has grown into a leading regional healthcare system. Say hello to a relaxed lifestyle that empowers you to prioritize both your professional growth and family time. YRMC extends this inviting spirit within our walls, fostering a strong sense of family, and belonging among our team members. Come experience the exceptional quality of life that YRMC and Prescott offer. Work at the heart of #hellohumankindness and discover where your career and well-being truly connect. Job Summary and Responsibilities As our Acuity Adaptable ICU Nurse you will help patients with varying acuity levels by providing exceptional care, monitoring their condition, administering medications and treatments as prescribed by physicians, and ensuring that patients receive the necessary care and support to achieve optimal outcomes. Every day you will work in various units, such as ICU, PCU, and Med-Surg, providing exceptional care to patients with varying acuity levels. You will be expected to monitor and manag ### Prescribing Physicians Psychiatrist - Virtual High Acuity Care - Part-time (W2) - Lyra Health - Location: United States (unspecified) - Salary: Not disclosed - Posted: 2026-04-01 - 401(k) match: 3% (not source-backed) - Mental health support: yes (not source-backed) - Apply: https://jobs.lever.co/lyrahealth/8cabe94d-ca99-433a-9143-d659720eddd6 - Excerpt: Prescribing Physicians Psychiatrist - Virtual High Acuity Care - Part-time (W2) United States About Lyra Lyra Clinical Associates partners with Lyra Health, a leading provider of evidence-based mental health care, serving more than 20 million people globally in partnership with employers and more than 100 million through health plan and partner relationships. The company has delivered more than 15 million sessions of mental health care, published more than 35 peer-reviewed studies, and delivered unmatched outcomes in terms of access, clinical effectiveness, and cost efficiency. Lyra members have access to care in one day, and nine out of ten improve with the support of providers like you. Lyra is transforming access to life-changing mental health care through Lyra Empower, the only fully integrated, AI-powered platform combining the highest-quality care and technology solutions. You will be employed by Lyra Clinical Associates. About the Role Lyra Health is seeking a dedicated and experienced part-time psychiatrist to provide crucial psychiatric support to the following virtual high acuity care services: Lyra's Pediatric virtual Intensive Outpatient Program (vIOP) for young people ages 7 to 25 Lyra's Dialectical Behavior Therapy program for adults and teens Lyra Renew is our substance use disorder (SUD) program for adults This is an excellent opportunity to join a dynamic and innovative team, delivering high-quality, evidence-based care to individuals in a virtual group setting. As a part-time High Acuity Care psychiatrist, you will collaborate closely with therapists and other members of the care team to provide comprehensive and integrated treatment. About the ### Director, Acuity Review Manager | Technology - FTI Consulting - Location: 7 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://fticonsulting.wd108.myworkdayjobs.com/fticonsultingcareers/job/Washington-DC/Director--Acuity-Review-Manager---Technology_JR26087-TEE - Excerpt: Director, Acuity Review Manager | Technology 7 Locations posted: Posted Yesterday ### ACM Consultant (S), Emp Svcs-G A&Accessibility VAR - Amazon - Location: USA (unspecified) - Salary: $20-$35/hr - Posted: 2026-06-08 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Fertility benefits: yes (not source-backed) - Adoption assistance: yes (not source-backed) - Mental health support: yes (not source-backed) - Childcare support: yes (not source-backed) - Apply: https://www.amazon.jobs/en/jobs/10442475/acm-consultant-s-emp-svcs-g-a-accessibility-var - Excerpt: ACM Consultant (S), Emp Svcs-G A&Accessibility VAR USA Application deadline: Applications will be accepted on an ongoing basis At Amazon we believe that every day is still day one. We are working to be the most customer-centric company on earth. To get there, we need exceptionally talented, bright, and driven people. If you'd like to help the Disability Leave Services (DLS) team build a best-in-class professional services program to deliver leave of absence, disability and accommodation services to Amazon employees, applicants, job seekers and candidates globally, this is your chance to make history by joining the amazing Disability & Leave Services Team. The ACM Consultant provides case management for all types of accommodation request related to life events. The ACM Consultant is highly skilled in answering questions, understanding the employee's situation, applying the appropriate benefits, responding to changing circumstances and needs, and paves the way for a connected and trusted case management experience. Case Managers are the single point of contact for an employee throughout an entire leave of absence or disability event. Key job responsibilities • Initiate and respond to inquiries about accommodation events, benefits, and options available to employees • Serve as a point of contact for assigned employees to provide holistic case management services, including reviewing medical documentation in compliance with the corresponding, federal and state laws and policy as defined by Amazon • Leverage duration guidelines, best practice tools and Amazon resources to support oversight of aan accommodation as appropriate • Critically assess and adjust the ### Neuroscience Sales Specialist - San Jose, CA - Acadia Pharmaceuticals Inc - Location: California - Remote (remote) - Salary: $124K-$155K - Posted: 2025-12-15 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### Director Drug Safety & Pharmacovigilance Medical Safety - Acadia Pharmaceuticals Inc - Location: Princeton, New Jersey, United States (unspecified) - Salary: $221K-$276K - Posted: 2026-04-23 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### Associate Director, Quality Operations - Acadia Pharmaceuticals Inc - Location: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) - Salary: $145K-$181K - Posted: 2026-05-28 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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, ### Senior Director, Patient Support Service Operations & Solutions - Acadia Pharmaceuticals Inc - Location: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) - Salary: $227K-$284K - Posted: 2026-06-08 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### Neuroscience Sales Specialist - Southern New Jersey, NJ - Acadia Pharmaceuticals Inc - Location: New Jersey - Remote (remote) - Salary: $92K-$115K - Posted: 2026-05-19 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### Senior Medical Director - Celcuity - Location: Remote (remote) - Salary: $260K-$350K - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/celcuity/jobs/4112168009 - Excerpt: Senior Medical Director Remote Position Summary: We are seeking a Senior Medical Director who will report into the Vice President, Clinical Development. You will be responsible for working within Celcuity's medical team providing medical oversight of service suppliers driving on-going clinical studies and plans and executes the study design protocol development, implementation and monitoring of the company's new Phase I-III Oncology clinical trials. The position will provide key overall clinical, scientific and/or logistical support to clinical development programs and is responsible for the compliance of the department and the company to regulatory standards and procedures. Responsibilities: Assist in design, author and/or review clinical study synopses, protocols, amendments, study reports and other study-related documents. Act as a medical monitor for assigned study. Discuss study design with investigators and key opinion leaders. Provide clinical input for clinical protocol monitoring guidelines and analysis plans. Drive clinical database design, data collection and cleaning and oversees clinical interpretation of study data. Track emerging efficacy and safety profile of drugs in on-going clinical trials; inform Clinical Development team of changes in the efficacy/safety and/or risk benefit profiles as they occur. Provide input and/or prepare clinical sections of regulatory documents (e.g., INDs, IND annual reports, Investigator's Brochures, CRFs, Informed Consent forms, Statistical Analysis Plans, Data Management edit check specs, clinical supplies package diagrams and labeling). Lead or assist in the development of publications - abstracts, manuscripts, slides, etc. In collaboration with team members (e.g., Clinical Operations, Data Management), assist in identifying / evaluating / monitoring vendors, monitoring ### Director, Clinical Quality Assurance (CQA) - 4D Molecular Therapeutics Inc - Location: Remote, United States (remote) - Salary: $205K-$235K - Posted: 2026-04-22 - Apply: https://4dmoleculartherapeutics.com/careers/?gh_jid=4687837005 - Excerpt: Director, Clinical Quality Assurance (CQA) Remote, United States Attention recruitment agencies: All agency inquiries are vetted through 4DMT's internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future. 4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company's lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company's lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company's second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery GENERAL SUMMARY The Director of Clinical Quality Assurance (CQA) will be responsible for Quality Assurance oversight of multiple, global, 4DMT sponsored clinical trials, ensuring trials are executed in compliance with all applicable international regulatory requirements for Good Clinical Practice (GCP). This position reports to the Senior Director, GCP Compliance and Quality Systems and ### CRM Developer / Administrator - Ocular Therapeutix Inc - Location: United States (unspecified) - Salary: $160K-$170K - Posted: 2026-05-06 - 401(k) match: listed (not source-backed) - Apply: https://www.ocutx.com/careers/open-positions/5130151007?gh_jid=5130151007 - Excerpt: CRM Developer / Administrator United States Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space. Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity. I. Position Summary: Reporting to the Sr Director, Data Strategy & Analytics, this role is responsible for supporting the implementation and integrations of large data assets and analytics into the Ocular CRM. Work with the Sr Director, Data Strategy & Analytics to optimize all reporting platforms. The Sr Associate, Business Analytics must be able to work in a matrix organization to compliantly address the analytical needs of his/her internal customers. II. Principal Duties and Responsibilities include the following: - Lead configuration, customization, maintenance, and support in the effective assessment, development, delivery, and usage of Ocular's CRM application for Field Sales, Reimbursement and Medical teams. - Design, develop, deploy, provide end user support, and maintain dashboards, reports, user roles, security, profiles, workflow rules, etc. while integrating the team's business needs into Veeva CRM. - ### Quality Assurance Manager - Medical Devices - AbbVie Inc. - Location: Sligo, SO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012313546-quality-assurance-manager-medical-devices - Excerpt: Quality Assurance Manager - Medical Devices Sligo, SO, Ireland 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: AbbVie invites you to join our cutting-edge pharmaceutical facility in Sligo, nestled in a region known for its vibrant community and scenic beauty. Embrace an opportunity to grow your career while contributing to meaningful innovations that enhance global health. An exciting role has opened up on our Ballytivnan site in Sligo. We are currently looking for a Quality Manager overseeing the Medical Device Quality team, reporting to the Quality Site Head. You will oversee the whole quality function for the medical device business on site. You'll ensure compliance with quality standards and regulatory requirements, leading a dedicated team of quality professionals. Responsibilities Quality Assurance & Control: Oversee testing of raw materials, manufacturing quality control, and product validation. Team Leadership: Manage and lead a team responsible for compliance and quality oversight. Regulatory Compliance: Ensure adherence to corporate and regulatory requirements. Performance Reporting: Report on the performance of the quality management system to senior management. Issue ### Optometrist (Clinical) - Department of Defense - Location: Fort Bragg, North Carolina (unspecified) - Salary: $128K-$166K - Posted: 2026-06-02 - Hires in: NC - Apply: https://www.usajobs.gov:443/job/871215900 - Excerpt: Optometrist (Clinical) Fort Bragg, North Carolina Summary About the Position: This position serves as a primary eye care provider, with emphasis on therapeutic pharmaceutical agents, medical contact lens specialist, operative refractive surgery management, and is located with Womack Army Medical Center's, at Fort Liberty NC. This is a Direct Hire Solicitation. Salary negotiation may be available for those candidates who are new to Federal service. A recruitment or relocation incentive may be authorized. Student Loan repayment may be authorized. Duties Serve as a primary eye care provider on therapeutic pharmaceutical agents, medical contact lens specialist, pre and post operative refractive surgery management, and consultations of Occupational Health through examinations of personnel. Identify systemic problems in addition to visual/ocular problems. Follow quiescent and slowly progressive ocular conditions as long as no medical or surgical intervention is indicated. Treat a full range of eye and visual problems and ocular diseases, to include the application of advanced instrumentation, optometric procedures and techniques. Monitor the maintenance of ophthalmic equipment and instruments. Perform comprehensive/limited visual and ocular examinations on all types of patients; including, but not limited to refractive surgery, pediatrics, adults, geriatric, learning disability, low vision, contact lens, and eye hazardous occupations. Diagnose and treat any visual anomaly and specified pathologic conditions of the ocular adnexa and the eye. Provide supervision, teaching, and guidance to senior optometric interns/Scholarship Program Students, eye specialist students, and/or eye technicians. Perform full range of professional optometric duties with major emphasis in the pre-operative evaluation of refractive surgery patients ### Product Specialist Eye Care - Emirati Nationals - AbbVie Inc. - Location: Remote | Abu Dhabi, Abu Dhabi, United Arab Emirates (remote) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012564856-product-specialist-eye-care-emirati-nationals - Excerpt: Product Specialist Eye Care - Emirati Nationals Remote | Abu Dhabi, Abu Dhabi, United Arab Emirates 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: Health Care providers (HCP) relationship management Delivers expected performance and beyond in the territory for AbbVie portfolio. Creates a pre-call plan using SMART objectives & effectively evaluates calls and documents post-call. Uses evidence-based medicine skills during the call (clinical papers etc.); promotes visually by appropriate use of currently approved promotional aids. Effectively handles objections or concerns. Consistently gains a logical, reasonable call to action/close on every call. Educates medical providers and staff. Identifies, develops, and maintains disease state experts and speakers/advocates. Utilizes innovative approaches and resources to gain access to difficult to see HCPs and elevates results and outcomes to the brand team level through his/her Field Manager. Differentiates AbbVie's value proposition to all health providers assigned. Continuously strive to gain market intelligence: insights on HCP needs, expectations and environmental challenges, which are shared across the in-field teams and leverage to the Brand teams (e.g. dedicates significant effort to the questioning stage ### Hardware Health - Microsoft - Location: US (unspecified) - Salary: Not disclosed - Posted: 2025-11-25 - 401(k) match: listed (not source-backed) - Apply: https://apply.careers.microsoft.com/careers/job/1970393556629383 - Excerpt: Hardware Health US ### Precision Medicine Director - Novartis - Location: Barcelona Barberà (unspecified) - Salary: Not disclosed - Posted: 2026-06-08 - 401(k) match: listed (not source-backed) - Apply: https://novartis.wd3.myworkdayjobs.com/Internal_Careers_for_Acquired_Entities/job/Barcelona-Barber/Precision-Medicine-Director_REQ-10080335-1 - Excerpt: Precision Medicine Director Barcelona Barberà posted: Posted 4 Days Ago ### Senior Product Manager, Acuity Scheduling, (Classes) - Squarespace - Location: New York City (unspecified) - Salary: $154K-$247K - Posted: 2026-04-01 - Parental leave: 12 weeks (not source-backed) - Fertility benefits: yes (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: http://www.squarespace.com/about/careers?gh_jid=7699712 - Excerpt: Senior Product Manager, Acuity Scheduling, (Classes) New York City At Squarespace, we empower product teams to solve meaningful customer and business problems. We're looking for a Senior Product Manager to lead Acuity's Classes product, the team responsible for enabling group-based businesses to sell, manage, and scale ad hoc and recurring, one-to-many experiences. Classes supports customers who run group sessions, workshops, fitness classes, courses, and events. These sellers have fundamentally different needs than 1:1 appointment businesses, including capacity management, cohort pricing, attendance tracking, flexible enrollment, and scalable checkout. Today, Classes remains an early-stage product with significant untapped potential. This role will define what Classes can become and build the foundation for durable, long-term growth. This role requires a highly rigorous approach to problem definition. You will be expected to deeply understand customer needs, business opportunities, and market dynamics before proposing solutions. Success in this role means consistently anchoring product decisions in validated problems, not inherited workflows or legacy systems. This is a hybrid role, requiring 1-3 days a week in our New York City office. You will report to the Senior Group Product Manager on the Acuity Scheduling team. You'll Get To... - Own the long-term strategy and roadmap for Acuity's Classes and group-booking products - Lead deep problem discovery to clearly define customer, market, and business opportunities before pursuing major investments - Develop strong, evidence-based problem statements grounded in user research, data, and competitive analysis - Define clear target segments, primary use cases, and expansion opportunities for class-based sellers - ### Sr. Manager, R&D AI Solutions & Analytics - 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 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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, ### Director, Clinical Quality Assurance - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013409536-director-clinical-quality-assurance - Excerpt: Director, Clinical Quality Assurance North Chicago, IL, 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: Purpose : AbbVie is dedicated to delivering a consistent stream of innovative, safe, and effective medicines and products that solve serious health issues and have a remarkable impact on people's lives. As a quality organization in research & development, R&D Quality Assurance (RDQA) is committed to driving quality excellence across all stages of discovery and development for the product's lifecycle to achieve product realization and accelerate access to innovative therapies and products for our patients. Patient needs, stakeholder demands, industry innovation, regulatory landscape, and AbbVie's evolved business strategy are complex, rapid pace, and dynamic. Emphasizing and embedding quality in the execution of clinical trials ensures data integrity, fosters regulatory compliance, and contributes to the overall success of drug/device development programs. The Director, Clinical Quality Assurance is responsible for developing and implementing global strategic quality oversight for Therapeutic Areas (TAs) within clinical development programs. This role ensures that R&D complies with corporate policies and worldwide ### Optician - CACI - Location: Danbury, CT, US (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://caci.wd1.myworkdayjobs.com/External/job/Danbury-CT-US/Optician_324365 - Excerpt: Optician Danbury, CT, US posted: Posted 30+ Days Ago ### Neuroscience Sales Specialist - Allentown, PA - Acadia Pharmaceuticals Inc - Location: Pennsylvania - Remote (remote) - Salary: $92K-$115K - Posted: 2026-06-09 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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. - ### Supervisory Optometrist - Department of Health and Human Services - Location: Multiple Locations (unspecified) - Salary: $170K-$221K - Posted: 2026-06-09 - Hires in: AZ, ND, NM, SD - Apply: https://www.usajobs.gov:443/job/872356300 - Excerpt: Supervisory Optometrist Multiple Locations Summary We are pleased to announce an exciting opportunity for a dedicated Supervisory Optometrist to join our healthcare team. This leadership role provides comprehensive eye care services, oversees clinical operations, and promotes quality patient outcomes. As a key member of the organization, you will help advance ocular health and improve access to care while leading a team committed to excellence and service for Native American communities. Duties Plan, implement and direct the optometry eye care program. Establish and maintain working policies of the eye clinic, assure adequate staffing of the optometry clinic; develop or direct the development of procedure manuals for the optometry program and establish and maintain effective quality control and performance improvement. Directs the full range of ocular testing and examinations from a clinical as well as an administrative point of view. Treats visual disorders through the prescription of corrective lenses and vision training and pharmacological means. Provide orientation and training for facility personnel, coordinate all professional continuing education for eye care personnel, and monitor all completion of mandatory training for eye care personnel. Assists with provision of screening programs, kindergarten school screening and diabetic retinopathy. Develop, evaluate and revise performance improvement programs to evaluate quality, appropriateness and effectiveness of eye care services provided. Ensure that the performance improvement program is in compliance with Optometry, Service Unit, and IHS and Joint Commission standards. Participate in service unit performance improvement planning. The selected individual is required to obtain and maintain medical staff clinical privileges, including ### ACM Consultant (S), Emp Svcs-G A&Accessibility VAR - Amazon - Location: USA (unspecified) - Salary: $20-$35/hr - Posted: 2026-06-01 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Fertility benefits: yes (not source-backed) - Adoption assistance: yes (not source-backed) - Mental health support: yes (not source-backed) - Childcare support: yes (not source-backed) - Apply: https://www.amazon.jobs/en/jobs/10435529/acm-consultant-s-emp-svcs-g-a-accessibility-var - Excerpt: ACM Consultant (S), Emp Svcs-G A&Accessibility VAR USA Application deadline: Jun 16, 2026 At Amazon we believe that every day is still day one. We are working to be the most customer-centric company on earth. To get there, we need exceptionally talented, bright, and driven people. If you'd like to help the Disability Leave Services (DLS) team build a best-in-class professional services program to deliver leave of absence, disability and accommodation services to Amazon employees, applicants, job seekers and candidates globally, this is your chance to make history by joining the amazing Disability & Leave Services Team. The ACM Consultant provides case management for all types of accommodation request related to life events. The ACM Consultant is highly skilled in answering questions, understanding the employee's situation, applying the appropriate benefits, responding to changing circumstances and needs, and paves the way for a connected and trusted case management experience. Case Managers are the single point of contact for an employee throughout an entire leave of absence or disability event. Key job responsibilities • Initiate and respond to inquiries about accommodation events, benefits, and options available to employees • Serve as a point of contact for assigned employees to provide holistic case management services, including reviewing medical documentation in compliance with the corresponding, federal and state laws and policy as defined by Amazon • Leverage duration guidelines, best practice tools and Amazon resources to support oversight of aan accommodation as appropriate • Critically assess and adjust the case management plan to an ### Sr. Health Systems Manager - Texas - Acadia Pharmaceuticals Inc - Location: Texas - Remote (remote) - Salary: $158K-$197K - Posted: 2026-04-29 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### Associate Director, Computer System Validation & Quality Compliance - Amylyx Pharmaceuticals Inc - Location: Cambridge, MA (unspecified) - Salary: $170K-$191K - Posted: 2026-03-09 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/amylyx/jobs/5818910004 - Excerpt: Associate Director, Computer System Validation & Quality Compliance 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 Associate Director, Computer System Validation (CSV) & Quality Compliance provides enterprise‑level leadership, strategic direction, and governance for the validation, lifecycle management, and continuous compliance of GxP‑relevant computerized systems, with a strong emphasis on the Veeva Quality Suite. This role ensures that digital quality solutions and supporting systems meet global regulatory requirements (FDA, EMA, ICH, GAMP 5), maintain data integrity, and enable a sustainable, inspection‑ready state across the organization. This person will partner closely with Quality, IT, Regulatory, Clinical, and business process owners to define system requirements, lead new system implementations and major enhancements, and drive harmonized, risk‑based validation practices. This role also oversees quality compliance processes ### Sr. Medical Director, Pharmacovigilance - Maplight Therapeutics Inc - Location: Remote (remote) - Salary: $319K-$361K - Posted: 2025-12-09 - Apply: https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5025985008 - Excerpt: Sr. Medical Director, Pharmacovigilance Remote 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: The Senior Medical Director, Pharmacovigilance will lead the medical safety evaluation and benefit-risk assessment for products throughout their lifecycle with focus on patient well-being and compliance and applicable regulatory requirements. This person will lead cross-functional safety management team (SMT) and collaborate with other members Clinical Development and Medical Affairs (CDMA), contract research organizations (CROs), and drug development collaborators/partners to ensure that all clinical safety and benefit-risk assessment is performed adequately for assigned products. Reporting to the Vice President, Pharmacovigilance, the Senior Medical Director will oversee cross-functional teams and may have direct reports Responsibilities: - Lead product safety surveillance and oversee evolving safety and benefit-risk profiles for assigned products. - Lead cross-functional safety management team (SMT) for assigned products, and responsible for the on-going assessment of benefit-risk profiles and related actions during the product life cycle. - Review safety data from various sources (e.g. pre-clinical, clinical trial data, post-marketing, literature) throughout the development process as well as post marketing for assigned products. - Responsible for conducting signal detection activities, monitoring, evaluation, interpretation and appropriate management and communication of safety information - Represent pharmacovigilance on cross-functional product/project teams including review of safety sections of protocols, investigator brochures, informed ### General Application - AbbVie Inc. - Location: İstanbul, İSTANBUL, Turkey (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990007535959-general-application - Excerpt: General Application İstanbul, İSTANBUL, Turkey 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 Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description: General Application Unleashing your untapped potential? We Offer That. 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, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. If you are interested in being part of AbbVie Turkey Team but have not found a specific role fitting for you, leave your application here and you will be included in our databases. Qualifications: Qualifications: University degree Good command of written and spoken English High capability in interpersonal skills - strong negotiation skills with a problem-solver mind Ability to build and maintain relationships and work confidently with people at all levels This is for General Applications. We will keep your applications in our files for future job opportunities. We make your continuous learning and development a top priority, so ### Director, Clinical Quality Assurance - Corcept Therapeutics - Location: Redwood City, California, United States (unspecified) - Salary: $229K-$260K - Posted: 2026-05-13 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5995887004 - Excerpt: Director, Clinical Quality Assurance Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Director of Clinical Quality Assurance (CQA) is a senior member of the CQA team and will lead and perform day-to-day clinical quality operations and compliance activities to support the success of the clinical studies sponsored or supported by Corcept. This is a hybrid role typically requiring on-site presence at least 3 days per week. Responsibilities: - Lead Clinical Quality Assurance activities as line manager to assigned CQA Leads and working with therapeutic area teams to support success of the clinical studies sponsored or supported by Corcept - Champion and influence management and growth of the Clinical Quality Assurance team with the goal of attracting and developing talent, creating a rewarding professional environment, and ensuring that the team's capabilities meet Corcept's future needs - Lead, manage, and train others on GCP audits, including clinical investigative site audits, clinical ### Field Reimbursement Manager - Oral Migraine - AbbVie Inc. - Location: Remote | Pittsburgh, PA, United States (remote) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013579266-field-reimbursement-manager-oral-migraine - Excerpt: Field Reimbursement Manager - Oral Migraine Remote | Pittsburgh, PA, 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 Field Reimbursement Manager (FRM) - Neuroscience acts as an alternative in-office resource that is available to address HCP questions about patient access. The FRM calls directly on HCP offices in their assigned, specific geography to answer questions about patient access & reimbursement in support of the AbbVie Neuroscience portfolio. The FRM provides expertise on coverage and common access and reimbursement challenges affecting AbbVie Neuroscience products. The FRM responsibilities include educating on the access and reimbursement support tools available from AbbVie, advising HCPs on patient prescription status and program eligibility, and educating HCP offices on payer processes and procedures. Specific Responsibilities: Educate HCPs on patient support programs, including access and reimbursement support tools and services Educate on product-specific acquisition and access options such as specialty pharmacy networks and specialty distribution Educate on resources available to address access issues Provide local expertise in regards to national/regional payor policies in order to educate providers on payer issues, coding ### Associate Director R&D AI Solutions & Analytics - 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 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### Associate Director, Clinical Quality and Continuous Improvement - Alnylam Pharmaceuticals - Location: United States | Cambridge, MA, USA (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://alnylam.eightfold.ai/careers/job/893395304988 - Excerpt: Associate Director, Clinical Quality and Continuous Improvement United States | Cambridge, MA, USA ### Associate Director, Patient Services - Axsome Therapeutics - Location: New York, NY (unspecified) - Salary: $155K-$185K - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/axsometherapeutics/jobs/5779343004 - Excerpt: Associate Director, Patient Services New York, NY Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at www.axsome.com and follow us on LinkedIn and X . About This Role Axsome Therapeutics is seeking an Associate Director, Patient Services to lead the establishment and growth of a new Patient Services Hub. This role will work closely with the Director, Patient Services for developing, implementing, and overseeing all aspects of the Hub's operations, ensuring efficient and seamless patient access to therapies and support services. This role requires a strong leader to build and manage the hub team, foster collaborative relationships, and drive continuous improvement within a fast-paced environment. This role will have close collaboration among, and provide ad hoc support to, Field Access and Patient Service functions within the Market Access team, as related to the HUB. ### Manager, Commercial Analytics & Insights - Neuro - 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 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### MSL, Eyecare - AbbVie Inc. - Location: Tokyo, Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990011935116-msl-eyecare - Excerpt: MSL, Eyecare Tokyo, Tokyo, Japan 企業概要: 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. 求人内容: Objectives: Medical Science Liaisons (MSL) will ensure that proper relationships with both established and emerging external experts (EEs) in Ophthalmology and Eyecare disease treatment are developed and nurtured ,and that our scientific credibility is advanced as planned. This position is based in Tokyo and will report to the MSL Manager, Eyecare. Key Responsibilities: Develop and maintain key scientific knowledge for credible dissemination of Eyecare and Ophthalmology related scientific information to external experts and healthcare professionals. Identify qualified external experts to engage with in collaborative efforts such as Advisory Board meetings, medical educational programs, congress symposia and potential research collaborations. Conduct with high integrity infield activities as determined by the annual medical functional plan and properly document outcome of scientific engagements with targeted external experts. Provide scientific support to and maintain relationships with targeted external experts in Eyecare area including key academic societies by delivering credible scientific presentations through individual or in group interactions. Provide external ophthalmic surgical experts with scientific and technical support to ensure ### Patient Reported Outcomes Manager - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013456216-patient-reported-outcomes-manager - Excerpt: Patient Reported Outcomes Manager 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 Patient Reported Outcomes Manager reports to a Clinical Program Development (CPD) Program Lead and will be responsible for ensuring timely, adequate, cost effective business aligned standards, strategies and processes related to Patient Report Outcomes on behalf of the Clinical Development organization. Responsibilities Responsible for compliance with applicable Corporate and Divisional Policies and procedures. Provide project management and expert consultation supporting patient centered/PRO licensing and translation activities for all Therapeutic Areas within Clinical Program Development (CPD). Serve as the owner of the Vault PRO Library which is a repository for PROs and includes licensing and permission details & terms; MSAs with AbbVie; translation requirements; training requirements; electronic format requirements; etc. Interact with PRO owners, Outsourcing, HEOR, Data Sciences and the clinical teams to drive and facilitate the PRO and ePRO implementation with respect to vendor contract initiation, translation management, project milestones, timelines, and deliverables during Study Start up. Provide strategic & technical expertise and training to the CPD organization ### Director, Safety Scientist, Pharmacovigilance - Maplight Therapeutics Inc - Location: Remote (remote) - Salary: $220K-$240K - Posted: 2026-05-04 - Apply: https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5206405008 - Excerpt: Director, Safety Scientist, Pharmacovigilance Remote 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: The Safety Scientist will be responsible for high quality safety surveillance activities including medical review of individual case safety reports (ICSRs), aggregate report production, safety governance meeting coordination, safety signal detection and assessment, and safety risk management activities for assigned products. This individual will collaborate with Program Safety Lead and other program team members, pharmacovigilance operations, and CROs to ensure proactive safety surveillance in compliance with global regulations. Responsibilities: - Manage safety surveillance and signal detection activities (period review of aggregate safety data, safety surveillance team meetings, track signals and related documentation) - Represent PV at clinical study team for assigned product - Develop signal assessment report under the oversight of Program safety lead for validated safety signal - Collaborate with PV operations for timely and accurate medical review of ICSRs for assigned clinical study as needed - Develop and contribute safety risk management plan across product lifecycle - Develop and manage periodic reports (DSUR/PBRER) - Contribute for data analysis and authoring of safety sections for regulatory submissions and regulatory responses - Contribute for the development or updates of safety surveillance and risk management SOPs, templates etc. - Collaborate with clinical study teams on safety surveillance ### Sleep Center Specialist - Laureate Education INC - Location: Yale Campus - Hospital (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://saintfrancis.wd1.myworkdayjobs.com/External/job/Yale-Campus---Hospital/Sleep-Center-Specialist_JR29145-1 - Excerpt: Sleep Center Specialist Yale Campus - Hospital Yale Campus - Hospital ### Senior Associate R&D Quality and Risk Management - Acadia Pharmaceuticals Inc - Location: Princeton, New Jersey, United States (unspecified) - Salary: $32.21-$40.29/hr - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### User Experience (UX) Director - Coronary & Renal Denervation (CRDN) - Medtronic - Location: Galway, County Galway, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-02 - Parental leave: 24 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://medtronic.wd1.myworkdayjobs.com/medtroniccareers/job/Galway-County-Galway-Ireland/User-Experience--UX--Director---Coronary---Renal-Denervation--CRDN-_R64672-1 - Excerpt: User Experience (UX) Director - Coronary & Renal Denervation (CRDN) Galway, County Galway, Ireland posted: Posted 10 Days Ago ### Clinical Success Director (Pittsburgh) - Abridge - Location: PGH Office, Pittsburgh, Pennsylvania, USA (unspecified) - Salary: Not disclosed - Posted: 2026-01-28 - Apply: https://jobs.ashbyhq.com/abridge/0b93a993-d6b3-4f63-98ef-59969b342659 - Excerpt: Clinical Success Director (Pittsburgh) PGH Office, Pittsburgh, Pennsylvania, USA About Abridge Abridge was founded in 2018 with the mission of powering deeper understanding in healthcare. Our AI-powered platform was purpose-built for medical conversations, improving clinical documentation efficiencies while enabling clinicians to focus on what matters most-their patients. Our enterprise-grade technology transforms patient-clinician conversations into structured clinical notes in real-time, with deep EMR integrations. Powered by Linked Evidence and our purpose-built, auditable AI, we are the only company that maps AI-generated summaries to ground truth, helping providers quickly trust and verify the output. As pioneers in generative AI for healthcare, we are setting the industry standards for the responsible deployment of AI across health systems. We are a growing team of practicing MDs, AI scientists, PhDs, creatives, technologists, and engineers working together to empower people and make care make more sense. We have offices located in the Mission District in San Francisco, the SoHo neighborhood of New York, and East Liberty in Pittsburgh. The Role **Must be able to go into our Pittsburgh (East Liberty) office 3x/week. As a Clinical Success Director, you will be at the forefront of delivering an exceptional generative AI platform for clinicians. Your work will directly contribute to improving the cognitive burden associated with clinical documentation. You will collaborate with clients, partners, product managers, designers, machine learners, and healthcare professionals to bring to life products that bridge the gap between clinical conversations and actionable data. What You'll Do - Provide clinician enablement by delivering education and ### Associate Director, Clinical Data Programmer - Amylyx Pharmaceuticals Inc - Location: Cambridge, MA (unspecified) - Salary: $183K-$206K - Posted: 2026-03-05 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/amylyx/jobs/5763048004 - Excerpt: Associate Director, Clinical Data Programmer 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 Clinical Data Management team at Amylyx Pharmaceuticals is seeking an Associate Director, Clinical Data Programmer. This individual will work collaboratively cross-functionally to provide hands-on data management support, programming support and technical leadership to develop, maintain, validate the clinical database, and run computer programs that access, visualize, and report clinical trial data, in accordance with various clinical plans, ICH guidelines, and applicable regulatory requirements. As an Associate Director of Clinical Data Programming, you will be required to program in the appropriate languages to create both textual and graphic displays that facilitate data cleaning and review. Responsibilities - Lead the study-specific design, development, and validation of study clinical data capture systems, ### Rare Bone and Endocrine Medical Advisor - AstraZeneca - Location: Israel - Kfar Saba (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Israel---Kfar-Saba/Rare-Bone-and-Endocrine-Medical-Advisor_R-250448-2 - Excerpt: Rare Bone and Endocrine Medical Advisor Israel - Kfar Saba posted: Posted 30+ Days Ago ### Long-Term Care Sales Specialist - Central Michigan - Acadia Pharmaceuticals Inc - Location: Michigan - Remote (remote) - Salary: $92K-$115K - Posted: 2026-05-22 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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. - ### Patient Safety Group Manager - Novartis - Location: 2 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://novartis.wd3.myworkdayjobs.com/Internal_Careers_for_Acquired_Entities/job/Beijing-Beijing/Patient-Safety-Group-Manager_REQ-10061108 - Excerpt: Patient Safety Group Manager 2 Locations posted: Posted 30+ Days Ago ### Clinical Success - Nursing (Central Time Zone) - Abridge - Location: Remote - Tier 2, Remote - Tier 3 (remote) - Salary: Not disclosed - Posted: 2026-01-09 - Mental health support: yes (not source-backed) - Apply: https://jobs.ashbyhq.com/abridge/0576c283-9004-499a-9c1d-b2586b92b2b7 - Excerpt: Clinical Success - Nursing (Central Time Zone) Remote - Tier 2, Remote - Tier 3 About Abridge Abridge was founded in 2018 with the mission of powering deeper understanding in healthcare. Our AI-powered platform was purpose-built for medical conversations, improving clinical documentation efficiencies while enabling clinicians to focus on what matters most-their patients. Our enterprise-grade technology transforms patient-clinician conversations into structured clinical notes in real-time, with deep EMR integrations. Powered by Linked Evidence and our purpose-built, auditable AI, we are the only company that maps AI-generated summaries to ground truth, helping providers quickly trust and verify the output. As pioneers in generative AI for healthcare, we are setting the industry standards for the responsible deployment of AI across health systems. We are a growing team of practicing MDs, AI scientists, PhDs, creatives, technologists, and engineers working together to empower people and make care make more sense. We have offices located in the Mission District in San Francisco, the SoHo neighborhood of New York, and East Liberty in Pittsburgh. The Role As the Clinical Success Director/Manager - Nursing, you will be at the forefront of defining, launching, and growing our generative AI platform for nurses. Your work will directly contribute to improving the cognitive burden associated with clinical documentation. You will collaborate with clients, partners, product managers, designers, machine learners, and healthcare professionals to bring to life products that bridge the gap between clinical conversations and actionable data. What You'll Do - Evaluate new product offerings and provide subject matter expertise ### Neuro Critical Care APRN/PA, Nights - Laureate Education INC - Location: Yale Campus - Hospital (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://saintfrancis.wd1.myworkdayjobs.com/External/job/Yale-Campus---Hospital/APRN--CNP-III--Inpatient-_JR23386 - Excerpt: Neuro Critical Care APRN/PA, Nights Yale Campus - Hospital Yale Campus - Hospital ### APRN/CNP I, Urgent Care, Admiral - Laureate Education INC - Location: Warren Clinic - Tulsa Admiral (unspecified) - Salary: Not disclosed - Posted: 2026-06-07 - 401(k) match: listed (not source-backed) - Apply: https://saintfrancis.wd1.myworkdayjobs.com/External/job/Warren-Clinic---Tulsa-Admiral/APRN--CNP-I--Shift---Urgent-Care_JR28885 - Excerpt: APRN/CNP I, Urgent Care, Admiral Warren Clinic - Tulsa Admiral Warren Clinic - Tulsa Admiral ### APRN/CNP I, Urgent Care, Admiral - Laureate Education INC - Location: Warren Clinic - Tulsa Admiral (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - 401(k) match: listed (not source-backed) - Apply: https://saintfrancis.wd1.myworkdayjobs.com/External/job/Warren-Clinic---Tulsa-Admiral/APRN-CNP-I--Urgent-Care--Admiral_JR28882 - Excerpt: APRN/CNP I, Urgent Care, Admiral Warren Clinic - Tulsa Admiral Warren Clinic - Tulsa Admiral ### Product Lead, Emergency Department - Ambience Healthcare - Location: San Francisco, California, United States (unspecified) - Salary: $240K-$285K - Posted: 2026-05-14 - 401(k) match: 3% (not source-backed) - Apply: https://jobs.ashbyhq.com/ambiencehealthcare/baea43d8-92eb-4a41-8746-0d42496091fc - Excerpt: Product Lead, Emergency Department San Francisco, California, United States About Us: Here at Ambience, we never set out to be just another scribe. We're building the AI intelligence platform that restores humanity to healthcare and drives meaningful ROI for health systems across the country. Our technology helps providers focus on delivering great care by removing the administrative burden that pulls them away from patients and away from their most impactful work. Ambience delivers real-time coding-aware documentation and clinical workflow support across ambulatory, emergency and inpatient settings at the top health systems in North America. Our teams operate relentlessly with extreme ownership to build the best solutions for our health system partners. We value candor, positivity and deep thought - and we expect a lot from each other because we know the problems we're solving truly matter. Ambience was ranked #1 for Improving the Clinician Experience in the KLAS Research Emerging Solutions Top 20 Report, recognized by Fast Company as one of the Next Big Things in Tech, named one of the best AI companies in healthcare by Inc., and selected as a LinkedIn Top Startup in 2024 and 2025. We're backed by Oak HC/FT, Andreessen Horowitz (a16z), OpenAI Startup Fund, and Kleiner Perkins - and we're just getting started. Summary Ambience is looking for an ED Product Manager to own our Emergency Department platform end-to-end: roadmap, clinician experience, and go-to-market strategy. The ED is one of healthcare's highest-acuity, highest-velocity environments - and the place where documentation burden is most acute. ### AMI & Clinical Specialist Manager - Benelux - AbbVie Inc. - Location: Hoofddorp, NH, Netherlands (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012243811-ami-clinical-specialist-manager-benelux - Excerpt: AMI & Clinical Specialist Manager - Benelux Hoofddorp, NH, Netherlands Company Description: About AbbVie At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit https://global.allerganaesthetics.com/. Follow Allergan Aesthetics on LinkedIn. Job Description: The AMI & Clinical Specialist (CS) Manager is responsible for leading, developing, and structuring the Clinical Specialist function in the Benelux to ensure high quality clinical support and strong execution of the Allergan Medical Institute (AMI) strategy in the field. This role drives the operational and organizational performance of the Clinical Specialist team, contributes to the adaptation of AMI priorities to the needs of the Benelux market, and ensures that educational initiatives effectively support customer engagement, capability building, and business objectives. The position also supports and manages local faculties, ensuring strong engagement, appropriate preparation, and high quality delivery of educational activities, and owns the planning and execution of AMI educational events in the market. The role combines people leadership, operational excellence, and strategic field insight, ensuring high standards of execution, full compliance with local regulations, and strong alignment with cross functional teams. Key Responsibilities 1. Clinical Specialist Team Management Lead, coach, and develop a team of 2 Clinical Specialists, ensuring high performance and continuous skills development. Define priorities, manage ### Manager, Access and Reimbursement Services - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013584986-manager-access-and-reimbursement-services - Excerpt: Manager, Access and Reimbursement Services North Chicago, IL, 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: Purpose The Access and Reimbursement Support Services Manager will effectively manage the support center in order to provide the highest level of service to patients, health care providers (HCP), and internal and external customers, ensuring that inbound and outbound calls and corresponding inquiries and issues are completed all in alignment with key performance indicators. This role will also drive continuous improvement initiatives for activities and products provided. Responsibilities: Lead a team of supervisors who manage operations to deliver superior customer service, driving world-class leadership and strong performance. Monitor department and employee productivity levels, identify opportunities to improve optimization and enable implementations and cost controls. Monitor internal programs, similar industry programs and regulatory guidance to ensure program relevance and compliance. Lead and mentor direct reports responsible for operations of designated AbbVie products. Provide recommendations regarding appropriate promotional and business practices. Develop and manage relationships with payors, providers, and customers. Partner with commercial business partners ### Director, Clinical Quality Risk & Portfolio Oversight - Alnylam Pharmaceuticals - Location: United States | Cambridge, MA (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://alnylam.eightfold.ai/careers/job/893395304989 - Excerpt: Director, Clinical Quality Risk & Portfolio Oversight United States | Cambridge, MA ### Senior Associate, Quality Assurance - Ocular Therapeutix Inc - Location: Bedford, MA (unspecified) - Salary: $109K-$121K - Posted: 2026-06-03 - 401(k) match: listed (not source-backed) - Apply: https://www.ocutx.com/careers/open-positions/5154874007?gh_jid=5154874007 - Excerpt: Senior Associate, Quality Assurance Bedford, MA Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space. Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity. Position Summary: The Senior Associate, QA will work in collaboration with all departments within Ocular, to provide the necessary Quality Assurance (QA) oversight for the production of Drug Products including support of end-to-end operations from technology transfer and clinical production all the way through commercialization. Additionally, they will be responsible for providing QA oversight of Quality Control (QC) activities to ensure compliance with applicable regulatory requirements (e.g., GMP, GLP) and internal quality standards. This role ensures that QC testing, documentation, and data integrity practices meet established procedures and support product quality and safety This individual will also be responsible for quality oversight and phase-appropriate cGMP guidance throughout the product lifecycle. Principal Duties and Responsibilities : - Provide QA support for activities associated with site operations, including in-house manufacturing activities as well as those ### 治疗领域经理-眼科治疗领域 - Roche Holding AG - Location: Shanghai, Shanghai, China's Mainland (unspecified) - Salary: Not disclosed - Posted: 2025-12-26 - Apply: https://roche.wd3.myworkdayjobs.com/roche-ext/job/Shanghai/-_202512-132783/apply - Excerpt: 治疗领域经理-眼科治疗领域 Shanghai, Shanghai, China's Mainland Join our team as a Therapeutic Area Manager in Ophthalmology, where you will drive academic promotion plans and enhance communication with key healthcare professionals. If you have a strong background in medical knowledge and cross-functional experience, we want to hear from you! ### Educator, Patient/Clinical Services - DaVita - Location: 03342 - Stamford Dialysis (unspecified) - Salary: Not disclosed - Posted: 2026-05-29 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://davita.wd1.myworkdayjobs.com/DKC_External/job/03342---Stamford-Dialysis/Educator--Patient-Clinical-Services_R0457123 - Excerpt: Educator, Patient/Clinical Services 03342 - Stamford Dialysis posted: Posted 14 Days Ago ### Supervisor, Clinical - Cardiac Telemetry Heart Failure - Laureate Education INC - Location: Yale Campus - Hospital (unspecified) - Salary: Not disclosed - Posted: 2026-06-03 - 401(k) match: listed (not source-backed) - Apply: https://saintfrancis.wd1.myworkdayjobs.com/External/job/Yale-Campus---Hospital/Supervisor--Clinical---Cardiac-Telemetry-Heart-Failure_JR25805 - Excerpt: Supervisor, Clinical - Cardiac Telemetry Heart Failure Yale Campus - Hospital Yale Campus - Hospital ### Medical Science Liaison / Sr Medical Science Liaison (North Central) - 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 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### Anaesthetics Ophthalmic Registrar - Birmingham - Pulse Active Stations Network - Location: Birmingham, West Midldands (unspecified) - Salary: Not disclosed - Posted: 2026-06-07 - Apply: https://job-boards.greenhouse.io/pulse/jobs/6655331003 - Excerpt: Anaesthetics Ophthalmic Registrar - Birmingham Birmingham, West Midldands ### Neuroscience Sales Specialist, Lafayette, LA - Acadia Pharmaceuticals Inc - Location: Louisiana - Remote (remote) - Salary: $92K-$115K - Posted: 2026-05-22 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### Account Consultant, Interventional Glaucoma - Cleveland, OH - AbbVie Inc. - Location: Remote | Cleveland, OH, United States (remote) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013337546-account-consultant-interventional-glaucoma-cleveland-oh - Excerpt: Account Consultant, Interventional Glaucoma - Cleveland, OH Remote | Cleveland, OH, 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: This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience. The Account Consultant position manages sales processes for AbbVie's therapeutic products in accordance with approved marketing plans. Assigned sales goals are achieved through consultative and value based selling techniques coupled with comprehensive account management while implementing the US Marketing Plan. Account Consultants provide technical product knowledge and support to ensure customer adoption of the product portfolio while delivering customer satisfaction. Effective use of sales and data resources will enhance productivity and provide growth to meet or exceed the franchise goals. Complies with required reports, requests, and promotional compliance and effectively manages AbbVie field assets. Responsibilities Promote a product to meet/exceed sales goals in community/private practices as well as hospitals/health systems. Identify/uncover customer needs (training, clinical, operational, reimbursement) and address with appropriate AbbVie resources. Expert delivery of anatomical/procedural information and ### LPN (Day Shift 6a-6p) *Must have Skills for a High Acuity Unit - Palm Valley Post Acute - Pacs Group Inc - Location: Location not specified (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://pacs.wd108.myworkdayjobs.com/pacs/job/Palm-Valley-Post-Acute/LPN--Day-Shift-6a-6p---Must-have-Skills-for-a-High-Acuity-Unit---Palm-Valley-Post-Acute_JR172204 - Excerpt: LPN (Day Shift 6a-6p) *Must have Skills for a High Acuity Unit - Palm Valley Post Acute Location not specified posted: Posted 2 Days Ago ### MSL/Sr MSL, Migraine (IA, MN, NE, and Central MO) - AbbVie Inc. - Location: Remote | Des Moines, IA, United States (remote) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012913499-msl-sr-msl-migraine-ia-mn-ne-and-central-mo- - Excerpt: MSL/Sr MSL, Migraine (IA, MN, NE, and Central MO) Remote | Des Moines, IA, 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 Medical Science Liaison is a field based scientific expert who strategically supports the scientific and business objectives of a designated therapeutic area across the product life cycle for a specific geography/territory. The Medical Science Liaison is the primary communicators of AbbVie science within a specific geography with healthcare professionals. The Medical Science Liaison combines strong strategic vision clinical expertise, therapeutic area awareness, serving as a conduit of information to a cross functional customer base internally within AbbVie. The Medical Science Liaison develops and maintains professional relationships with internal and external customers to provide comprehensive medical and scientific support to AbbVie initiatives in assigned therapeutic areas. The Medical Science Liaison facilitates the exchange of scientific information, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies. Responsibilities Focus on mastery of scientific content, materials, disease state and therapeutic area to establish themselves as a scientific expert. Identify, ### Sr. Associate, Data Management - Ocular Therapeutix Inc - Location: United States (unspecified) - Salary: $105K-$120K - Posted: 2026-05-06 - 401(k) match: listed (not source-backed) - Apply: https://www.ocutx.com/careers/open-positions/5130147007?gh_jid=5130147007 - Excerpt: Sr. Associate, Data Management United States Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space. Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity. Position Summary: Reporting to the Sr Director, Data Strategy & Analytics, this position will have the unique opportunity to support the management and implementation of transformations to the Ocular Data Management System and support the integration of large data assets and analytics into the Ocular CRM. This role will be responsible for working closely with the Commercial Operations team, and across the US Commercial Organization to further develop and support the Data Management strategy that is aligned with Ocular's organizational needs. This position will focus on developing new and managing existing processes for effective data management that will ensure the completeness, accuracy, legitimacy, and usability of the Ocular Data Warehouse. This position will also work closely external vendor partners that are responsible for assisting with the ongoing management of the Ocular Data Warehouse ### Senior Director, Patient Services - Amylyx Pharmaceuticals Inc - Location: Cambridge, MA (unspecified) - Salary: $253K-$285K - Posted: 2026-04-06 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/amylyx/jobs/5849964004 - Excerpt: Senior Director, Patient Services 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 of Patient Services will play a critical role in shaping how Amylyx supports patients throughout their treatment journey. This leader will design, build, and launch a best-in-class patient support program for our lead product candidate, ensuring that it reflects a commitment to supporting patient access, community education, and operational excellence. This individual will bring strategic vision and hands on leadership to create an integrated support program-from access and reimbursement solutions to patient education and continued on-treatment support. As a key leader in the commercial organization, this individual will partner with colleagues across market access, sales, and marketing, as well as cross functionally, to ensure a seamless and high ### Anaesthetics Ophthalmic Specialty Registrar - Birmingham - Pulse Active Stations Network - Location: Birmingham, West Midlands (unspecified) - Salary: Not disclosed - Posted: 2026-06-07 - Apply: https://job-boards.greenhouse.io/pulse/jobs/6655319003 - Excerpt: Anaesthetics Ophthalmic Specialty Registrar - Birmingham Birmingham, West Midlands ### Lead CRA - Maplight Therapeutics Inc - Location: Remote (remote) - Salary: $165K-$185K - Posted: 2026-05-06 - Apply: https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5211630008 - Excerpt: Lead CRA Remote 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: Reporting to the VP of Clinical Operations the Lead Clinical Research Associate will oversee an assigned MapLight study monitoring team to ensure monitoring quality and excellence in line with MapLight's Mission, Vision, and Values. This role will maintain site management and monitoring responsibilities for assigned sites in addition to study team level work. This role will collaborate closely with key cross-functional internal stakeholders, Clinical Operations, Clinical Development, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendor partners to ensure quality of monitoring conduct and oversight from study start up through close out. This is a highly collaborative and dynamic role within a fast paced and results-oriented environment. Responsibilities : - Lead and manage a team of Clinical Research Associates. - Provide line management for CRAs inclusive of performance management and career development. - Ensure CRAs are trained and maintain compliance with internal procedures and processes and regulatory requirements (GCP). - Support the Clinical Operations study team with CRA resourcing. - Maintain site management and monitoring responsibility for at least one site for the assigned study(ies). - Prepare for and conduct Pre-Study, Initiation, Interim and Closeout monitoring visits in accordance ### Optometrist - Department of Defense - Location: Camp Lejeune, North Carolina (unspecified) - Salary: $90K-$116K - Posted: 2026-01-16 - Hires in: NC - Apply: https://www.usajobs.gov:443/job/854686000 - Excerpt: Optometrist Camp Lejeune, North Carolina Summary About the Position: This is a Flyer Announcement for an Optometrist GS-0662-12 position with Atlantic Naval Medical Center Camp Lejeune. This is a Flyer Announcement - Resume, Transcripts, Licenses and Certificates need to be emailed to LCDR Kantar @ michael.kantar.mil@health.mil. Duties Serve as a professional clinical optometrist within Medical Treatment Facilities (MTF) for the Defense Health Agency (DHA), including Warfighter Refractive Surgery Centers, vision centers, and eye clinics. Support DoD workforce readiness and the provision of diagnostic and preventive care services provided in a highly specialized area of optometry, specifically that of military clinical management and the delivery of expert military vision care. Serves as a primary care provider for patients seeking ocular/vision care and is an essential member of the interdisciplinary military medical team. Provide comprehensive professional optometric services to active-duty military personnel, military families, and other eligible beneficiaries. Independently apply advanced technology, neuro-visual testing and traditional evaluation methods. Performs military vision screening and determines fitness for military duties, including accession for military services, qualification for special military duties, and fitness for military duty after eye injury or surgery. Determines the accommodative, refractive and binocular status of the eyes, and scope of visual function in general to determine the proper applications of lenses to accommodate patients' needs. Diagnoses and manages vision clarity problems. Education See Education Requirements Above Evaluation This is a Flyer Announcement - Resume, Transcripts, Licenses and Certificates need to be emailed to LCDR Kantar @ michael.kantar.mil@health.mil.. Please follow all instructions ### Qualified Person - Novartis - Location: Ivrea (unspecified) - Salary: Not disclosed - Posted: 2026-05-27 - 401(k) match: listed (not source-backed) - Apply: https://novartis.wd3.myworkdayjobs.com/Internal_Careers_for_Acquired_Entities/job/Ivrea/Qualified-Person_REQ-10073536 - Excerpt: Qualified Person Ivrea posted: Posted 16 Days Ago ### (Sr.) Clinical Specialist - AbbVie Inc. - Location: Remote | Wuhan, Hubei, China (remote) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012523767--sr-clinical-specialist - Excerpt: (Sr.) Clinical Specialist Remote | Wuhan, Hubei, China Company Description: About AbbVie At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit https://global.allerganaesthetics.com/. Follow Allergan Aesthetics on LinkedIn. Job Description: 1. Delivers In-Clinic Services Identifies educational need and develops recommendations to enhance clinical practice in aesthetic practices through delivering a bespoke educational journey for each HCP enrolled on a Facilitation Pathway, and based on the HCP's self-assessment of knowledge, skills, and confidence. Number of supported clinics/HCPs will be ~30 but aligned with Affiliate-level strategic need; HCPs will be selected through cross-functional alignment between the National Sales Manager and the AMI Lead. Establishes a bespoke AMI Infinity curricula-aligned Facilitation Pathway with the HCP in pursuit of supporting improved patient outcomes. Facilitation is hands-off and the HCP retains clinical judgement and responsibility for patient treatment. Focus will be Beginner and Intermediate HCPs, but other segments may require support as determined on educational need by the Area & Affiliate AMI Lead. Maintains a high level of service through reliable and timely follow-up after any interaction with HCPs and records all activity in VEEVA CRM to allow for KPI monitoring. 2. Supports Education via AMI Digital World As a fundamental part of the Facilitation Pathway ### Associate Medical Advisor - Bayer - Location: Ho Chi Minh City,Ho Chi Minh City,Vietnam (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://talent.bayer.com/careers/job/562949976846841 - Excerpt: Associate Medical Advisor Ho Chi Minh City,Ho Chi Minh City,Vietnam ### Manager, Data Analytics & Investigations - Acadia Pharmaceuticals Inc - Location: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) - Salary: $108K-$136K - Posted: 2026-04-24 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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, ### Associate Director, International Marketing Strategy Lead – Acute and Menstrual Migraine - AbbVie Inc. - Location: Mettawa, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013336697-associate-director-international-marketing-strategy-lead-acute-and-menstrual-migraine - Excerpt: Associate Director, International Marketing Strategy Lead – Acute and Menstrual Migraine 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: Role Summary: The Associate Director, Strategy Lead - Acute and Menstrual Migraine serves as a strategic, cross-functional leader accountable for shaping and aligning the marketing strategy across the Acute and Menstrual Migraine. This role provides leadership and direction to three Sr. Managers overseeing Menstrual Migraine, Acute, and PCP/Digital engagement, ensuring their work is integrated into a cohesive strategy that supports brand objectives, customer needs, and organizational priorities. Key Responsibilities: Lead the overall strategic direction for the Acute and Menstrual Migraine portfolio, ensuring strong alignment across brand, customer, and channel strategies. Prepare for a successful launch strategy for Menstrual Migraine for Aquipta and Ubrelvy. Manage and develop three direct reports Ensure integration of segment-specific plans into a unified portfolio strategy that maximizes reach, impact, and efficiency. Oversee development and execution of marketing initiatives across Acute and Menstrual Migraine, while enabling PCP and digital engagement strategies that strengthen portfolio performance. Translate market insights, customer feedback, ### Vice President, Drug Safety/Pharmacovigilance - Crinetics Pharmaceuticals INC - Location: Remote (remote) - Salary: $339K-$424K - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/Remote/Vice-President--Drug-Safety-Pharmacovigilance_JR000557 - Excerpt: Vice President, Drug Safety/Pharmacovigilance Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. 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 a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. 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. Join our team as we transform the lives of others. Position Summary: The Vice President of Drug Safety/Pharmacovigilance will be instrumental in supporting the growth of the organization as it continues to build the value of its current products and develop new products. The incumbent will design and develop the Global Crinetics Drug Safety and Pharmacovigilance system, ensuring adequate resourcing, efficient and compliant safety reporting, designing implementation of Safety Surveillance Programs, oversight of the safety profiles of Crinetics products and playing a leading role in safety risk management activities. Essential Job Functions and Responsibilities: These may include but are not limited to: Safety reporting processes. Ensure the accurate receipt and processing of safety assessment reports. Ensure that medical and causality assessments of all ### LPN (Part Time/PRN) *Must have Skills for a High Acuity Unit - Palm Valley Post Acute - Pacs Group Inc - Location: Location not specified (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://pacs.wd108.myworkdayjobs.com/pacs/job/Palm-Valley-Post-Acute/LPN--Part-Time-PRN---Must-have-Skills-for-a-High-Acuity-Unit---Palm-Valley-Post-Acute_JR172213 - Excerpt: LPN (Part Time/PRN) *Must have Skills for a High Acuity Unit - Palm Valley Post Acute Location not specified posted: Posted 2 Days Ago ### Data Analyst, Data Intelligence - Acrisure Innovation - Location: Grand Rapids, Michigan (onsite) - Salary: Not disclosed - Posted: 2026-03-16 - 401(k) match: listed (not source-backed) - Fertility benefits: yes (not source-backed) - Mental health support: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/acrisureinnovation/jobs/8464583002 - Excerpt: Data Analyst, Data Intelligence Grand Rapids, Michigan Data Analyst , Data Intelligence Austin, TX or Grand Rapids, MI (Onsite 4 days per week) Note: This is a full-time role and we do not offer C2C or C2H employment and are not able to sponsor visas for this position. About Acrisure Acrisure Enterprise Technology Group is where human expertise meets advanced technology. A global fintech leader, Acrisure empowers millions of ambitious businesses and individuals with the right solutions to grow boldly forward. Bringing cutting-edge technology and top-tier human support together, we connect clients with customized solutions across a range of insurance, reinsurance, payroll, benefits, cybersecurity, mortgage services - and more. In the last twelve years, Acrisure has grown in revenue from $38 million to almost $5 billion and employs over 19,000 colleagues in more than 20 countries. Acrisure was built on entrepreneurial spirit. Prioritizing leadership, accountability, and collaboration, we equip our teams to work at the highest levels possible. The Role The Data Intelligence team is chartered with advancing data driven decision making across Acrisure. As a member of the Data Intelligence Team, you will be responsible for leading the requirements gathering, design, implementation and delivery of reporting and analytics capabilities for Finance and Accounting Business Functions. You will be comfortable working across a wide variety of people including senior executive leadership, analysts, program management, and technical team members. Here are some of the ways in which you'll achieve impact: - Drive the development of efficient and reliable reporting and analytics ### MSL, 片頭痛領域部 - AbbVie Inc. - Location: Minato City, Tokyo, Japan (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012886006-msl- - Excerpt: MSL, 片頭痛領域部 Minato City, Tokyo, Japan 企業概要: 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. 求人内容: Objectives: The Medical Science Liaisons (MSL) will work cross functionally with several internal stakeholders such as Medical Therapeutic Area Lead, Medical Manager, Medical Advisor, Scientific Advisor and other MSL of the team, Medical Information team, Pharmacovigillance and Drug Safety Evaluation teams, The Brand Manager and Brand Team members to ensure proper relationship is developed, nurtured and AbbVie's scientific credibility is advanced with established and emerging external experts (EEs) in the therapeutic area of headache and migraine. This position is based in Tokyo and will report to the MSL Manager, Migraine. Key Responsibilities: Lead the development and maintenance of key scientific evidence and knowledge on AbbVie products for credible dissemination to external experts and healthcare professionals in the treatment of headache and migraine. Lead the identification of properly qualified external experts to engage with as determined by the medical functional plan as well as in collaborative efforts such as Advisory Board meetings, medical educational programs, congress symposia and potential research collaborations. Lead the scientific support ### Key Account Manager - Thyroid Eye Disease - Amgen - Location: Malaysia - Kuala Lumpur (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://amgen.wd1.myworkdayjobs.com/Careers/job/Malaysia---Kuala-Lumpur/Key-Account-Manager---Thyroid-Eye-Disease_R-240225 - Excerpt: Key Account Manager - Thyroid Eye Disease Malaysia - Kuala Lumpur posted: Posted 30+ Days Ago ### Director, Manufacturing - Acadia Pharmaceuticals Inc - Location: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) - Salary: $173K-$216K - Posted: 2026-04-06 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### Growth Associate - Clarion - Location: NYC Office | OnSite (onsite) - Salary: Not disclosed - Posted: 2026-06-10 - 401(k) match: listed (not source-backed) - Apply: https://jobs.ashbyhq.com/clarion/1e0e69f8-9fa4-4f78-8fdb-65b3543b6ebd - Excerpt: Growth Associate NYC Office | OnSite ABOUT CLARION The hardest part of healthcare shouldn't be getting an appointment. Today, medical staff drown in backlogs of calls, faxes, and scheduling requests. Patients struggle to get the right care at the right time, staff members burn out, and clinics lose billions in revenue. This isn't a failure of care - it's a failure of capacity. Clarion exists to solve this problem at scale. Our AI agents handle the patient journey from end-to-end; from scheduling and rescheduling appointments, to managing referrals and prescription refills. Our AI performs complex workflows with a human-like touch that patients love. We've raised $10M from Accel, Y Combinator, and Sequoia (Scout), along with founders from Ophelia, Medallion, and Counsel Health. We're an in-person team based in New York City, moving quickly to ensure every patient gets the care they need. WHY JOIN US? - Solving a real-world challenge: We're addressing a critical problem that affects millions of patients and providers daily. Our AI agents outperform human schedulers and restore the time needed to focus on patients. - Early-stage with strong market validation: We've seen 10x revenue growth in the last year alone. We handle millions of interactions for customers ranging from virtual care clinics to a $5B health insurance company. - Founding team: Our co-founders bring a deep understanding of the healthcare landscape. Our CEO is a Stanford/Harvard-trained physician and clinical ops leader (Two Chairs, Ophelia), and our CTO is an ex-Amazon Alexa engineer who led AI/ML teams ### DSM-RIN-广州 - AstraZeneca - Location: China (unspecified) - Salary: Not disclosed - Posted: 2026-06-03 - 401(k) match: listed (not source-backed) - Apply: https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/China/DSM-RIN-_R-253611 - Excerpt: DSM-RIN-广州 China posted: Posted 9 Days Ago ### ADHD NMP (Non-Medical Prescriber) - Pulse Active Stations Network - Location: London (unspecified) - Salary: Not disclosed - Posted: 2026-06-07 - Apply: https://job-boards.greenhouse.io/pulse/jobs/7524078003 - Excerpt: ADHD NMP (Non-Medical Prescriber) London ### Diagnostics Value Consultant - Liver diseases & navify Algosuite portfolio - Roche Holding AG - Location: Taipei, Taipei City, Taiwan (unspecified) - Salary: Not disclosed - Posted: 2026-04-17 - Apply: https://roche.wd3.myworkdayjobs.com/roche-ext/job/Taipei/Diagnostics-Value-Consultant---Liver-diseases---navify-Algosuite-portfolio_202604-109884/apply - Excerpt: Diagnostics Value Consultant - Liver diseases & navify Algosuite portfolio Taipei, Taipei City, Taiwan We are looking for a Diagnostics Value Consultant to advocate for diagnostic products in liver diseases and the Navify Algosuite portfolio. This role involves developing marketing strategies, engaging with healthcare professionals, and ensuring compliance with regulatory standards. Join Roche to make a significant impact in healthcare! ### Senior Specialist, Clinical Business Operations - Maplight Therapeutics Inc - Location: Burlington, MA (unspecified) - Salary: $115K-$135K - Posted: 2026-05-05 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5210932008 - Excerpt: Senior Specialist, Clinical Business Operations 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: MapLight is looking for a dynamic and experienced Senior Specialist, Clinical Business Operations. Reporting to the Executive Director, Clinical Operations, the Senior Specialist will be responsible for supporting all aspects of clinical business operations, including vendor selection, contracts, budget management and performance metrics. The ideal candidate will streamline operational procedures across multiple projects to improve timelines and organization of data. Responsibilities: - Vendor selection; including review and analysis, budget negotiations, development, and execution. - Manage the Request for Proposal (RFP) process. This includes: - Work with Clinical Trial Managers (CTM) and Clinical Scientific Leads to develop outsourcing strategy including range of vendors and timelines for award (i.e. schedule a vendor outsourcing strategy meeting). - Use the RFP template to customize to each study. - Create a draft of the RFP for review by the study team. - Communicate with vendors the RFP timelines and milestones and coordinate feedback to questions/answers. - Maintain the internal RFP timelines and milestones. - Following award, be the point of contact to receive the scope of work and budget grid from vendor. - Coordinate the review and consolidate the internal study team's (and finance) questions and comments regarding the ### Medical Assistant - Dermatology - Laureate Education INC - Location: Yale Campus - Warren Clinic Tower (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://saintfrancis.wd1.myworkdayjobs.com/External/job/Yale-Campus---Warren-Clinic-Tower/Medical-Assistant---Dermatology_JR28087 - Excerpt: Medical Assistant - Dermatology Yale Campus - Warren Clinic Tower Yale Campus - Warren Clinic Tower ### Senior Manager, Packaging and Serialization - Acadia Pharmaceuticals Inc - Location: Princeton, New Jersey, United States; San Diego, California, United States (unspecified) - Salary: $129K-$161K - Posted: 2026-03-03 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: 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 ### Supervisor, Clinical - Cardiac Telemetry - Laureate Education INC - Location: Yale Campus - Hospital (unspecified) - Salary: Not disclosed - Posted: 2026-05-23 - 401(k) match: listed (not source-backed) - Apply: https://saintfrancis.wd1.myworkdayjobs.com/External/job/Yale-Campus---Hospital/Supervisor--Clinical---Cardiac-Telemetry_JR28555 - Excerpt: Supervisor, Clinical - Cardiac Telemetry Yale Campus - Hospital Yale Campus - Hospital --- Source-backed benefit claims include source links; other benefit values are labeled separately.