# FewerJobs export - 100 curated jobs Generated: 2026-08-13T22:44:11.724Z Source: https://fewerjobs.com ## Filters applied - **q**: Amylyx Pharmaceuticals Inc - **quality_floor**: all - **match_401k_strict**: true - **parental_strict**: true - **non_birth_strict**: true - **pto_strict**: true - **include_older**: false - **apply_url_verified**: false - **page**: 1 - **per_page**: 100 - **sort**: relevance ## Jobs ### Director, Investor Relations - Amylyx Pharmaceuticals Inc - Location: Cambridge, MA (unspecified) - Salary: $204K-$230K - Posted: 2026-05-26 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/amylyx/jobs/6002934004 - Excerpt: Director, Investor Relations 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 Join Amylyx at a pivotal moment of growth and visibility as our Director, Investor Relations -a high-impact role at the center of our corporate story, strategy, and market presence. In this position, you'll work side-by-side with the VP of Investor Relations & Communications and partner closely with our senior leadership team-including our co-CEOs, CFO, CMO, and CCO-to shape how the investment community understands and values our mission. You'll serve as a strategic advisor and storyteller, helping to translate complex science and financial performance into a clear, compelling narrative that resonates with investors and analysts. You'll play a key role in strengthening our investor engagement program, building meaningful relationships, and influencing how Amylyx ### Process Engineer - Amylyx Pharmaceuticals Inc - Location: Cambridge, MA (unspecified) - Salary: $131K-$147K - Posted: 2026-05-27 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/amylyx/jobs/6002935004 - Excerpt: Process Engineer 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 Process Engineer, Drug Product, will provide technical and GMP support for contract manufacturing organizations (CMOs) responsible for late-stage clinical and commercial drug product supply. This role serves as the primary technical subject matter expert (SME) for aseptic processing including sterile filtration, formulation, filling, and container closure systems. The role will establish and maintain strong, trust-based relationships with CMO technical and quality teams to ensure reliable, compliant, and efficient manufacturing of aseptically filled drug products. Operating as a highly agile technical expert, partnering with CMOs and internal stakeholders to ensure robust execution across technology transfer, validation, and lifecycle management. This role reports to the Associate Director, CMC Drug Product. Responsibilities Commercial & Clinical ### 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 ### Senior Director, External Manufacturing - Amylyx Pharmaceuticals Inc - Location: Cambridge, MA (unspecified) - Salary: $245K-$276K - Posted: 2026-06-01 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/amylyx/jobs/6002938004 - Excerpt: Senior Director, External Manufacturing 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, External Manufacturing is a critical leadership role responsible for shaping and executing the external manufacturing strategy across clinical and future commercial programs. This individual will lead a global network of CDMO partners supporting a diverse and growing portfolio spanning peptides, oligonucleotides, and small molecules. As Amylyx advances toward commercialization and expands its global manufacturing footprint, this role will be instrumental in ensuring supply continuity, operational readiness, and long-term scalability. The Senior Director will partner cross-functionally to enable successful product launches, manage increasing manufacturing complexity, and build the infrastructure needed to support future growth and global expansion. Responsibilities - Provide strategic leadership and oversight of external manufacturing across clinical ### 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, ### Senior Director, Trade & Channel Operations - Amylyx Pharmaceuticals Inc - Location: Cambridge, MA (unspecified) - Salary: $255K-$287K - Posted: 2026-04-06 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/amylyx/jobs/5843909004 - Excerpt: Senior Director, Trade & Channel Operations Cambridge, MA Amylyx has an audacious mission to usher in a new era for treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitment to the communities we serve. We are a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS). Our mission is powered by our people. Our core values - be audacious, be curious, be authentic, be engaged, and be accountable - creating a culture of caring. Amylyx has assembled an experienced team ready to take action because the communities we serve have no time to wait. If you share our passion and are determined to tackle some of medicine's toughest problems, we encourage you to read the opportunity below and apply. The Opportunity The Senior Director, Trade & Channel Operations will be responsible for building Amylyx's U.S. distribution and channel model from the ground up in preparation for a future commercial launch of our lead product candidate. This individual will architect the distribution strategy, create the operational infrastructure necessary for launch, and partner cross functionally to ensure Amylyx is fully prepared to commercialize with excellence. As a key member of the Market Access team, this role will influence launch readiness, customer service delivery, and ongoing performance across distribution partners. Responsibilities - Design and build Amylyx's U.S. distribution model across specialty pharmacy, specialty distributor, and 3PL channels to support product launch - Lead ### Senior Vice President, Sales - Amylyx Pharmaceuticals Inc - Location: Flexible/ U.S. Based (unspecified) - Salary: $353K-$397K - Posted: 2026-05-13 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/amylyx/jobs/5994725004 - Excerpt: Senior Vice President, Sales Flexible/ U.S. Based Amylyx has an audacious mission to usher in a new era for treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitment to the communities we serve. We are a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS). Our mission is powered by our people. Our core values - be audacious, be curious, be authentic, be engaged, and be accountable - creating a culture of caring. Amylyx has assembled an experienced team ready to take action because the communities we serve have no time to wait. If you share our passion and are determined to tackle some of medicine's toughest problems, we encourage you to read the opportunity below and apply. The Opportunity The SVP of Sales will play a critical leadership role in building and executing the commercial strategy for a pre‑commercial biotechnology company preparing for its first product launch. This individual will be responsible for designing and implementing the Go‑To‑Market (GTM) strategy, recruiting and developing a high‑performing sales organization, establishing strong relationships with Key Opinion Leaders (KOLs), ensuring full sales force readiness ahead of launch and driving performance. We anticipate hiring the Senior Vice President, Sales in September 2026. The ideal candidate combines strategic vision with hands‑on execution experience in specialty pharma or biotech launches and thrives in a fast‑paced, build‑from‑scratch environment. Responsibilities Enterprise Commercial Leadership - Shape overall U.S. commercial ### Senior Medical Director, Clinical Development - Amylyx Pharmaceuticals Inc - Location: Cambridge, MA - Remote (remote) - Salary: $315K-$354K - Posted: 2025-07-29 - 401(k) match: listed (not source-backed) - Hires in: MA - Apply: https://job-boards.greenhouse.io/amylyx/jobs/5600871004 - Excerpt: Senior Medical Director, Clinical Development Cambridge, MA - Remote 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 Amylyx is seeking a Senior Medical Director, Clinical Development to provide strategic and scientific leadership for one or more late-stage, pivotal programs with the potential to expand into additional indications and/or programs within the same molecule or across the portfolio. This individual will play a critical role in shaping the overall clinical development strategy and may lead multiple programs or key components of a broader development portfolio. Reporting to the Senior VP of Clinical Development, you will be responsible for leading the design, execution, and interpretation of clinical studies and overseeing the development and implementation of Clinical Development Plans across assigned assets. You will provide strategic input into ### 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 ### Pharmaceutical Information Specialist,AI - Merck & Co., Inc. - Location: CHN - Shanghai - Shanghai (Tower A) (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Tower-A/Pharmaceutical-Information-Specialist-AI_R400237-1 - Excerpt: Pharmaceutical Information Specialist,AI CHN - Shanghai - Shanghai (Tower A) posted: Posted 7 Days Ago ### Biosample Manager - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: Not disclosed - Posted: 2026-05-02 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8444943002 - Excerpt: Biosample Manager Brisbane, CA Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Position: Biosample Manager Nurix Therapeutics, Inc. is seeking a Biosample Manager to join the Clinical Operations team. This is an onsite role. This individual will work cross functionally, with both internal and external stakeholders, to plan, coordinate, and oversee all operational activities required to manage the lifecycle of the clinical biosamples and support translational research. Responsibilities: Study Management - Provide guidance during protocol and informed consent form development to ensure logistical feasibility of biosample handling, alignment with planned analyses and ICH/GCP compliance - Participate in the CRF development process to ensure that biosample information is appropriately captured for sample tracking and reconciliation purposes - Serve as the functional lead as a member of the Clinical Study Teams and provide regular biosample metrics/trends and status updates - Partner with cross-functional teams to ensure timely delivery of biosample data to meet publication and study goals Biosample and Vendor ### Sr. Pharmaceutical Info Specialist - Merck & Co., Inc. - Location: CHN - Shanghai - Shanghai (Tower A) (unspecified) - Salary: Not disclosed - Posted: 2026-05-21 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Tower-A/Sr-Pharmaceutical-Info-Specialist_R399628 - Excerpt: Sr. Pharmaceutical Info Specialist CHN - Shanghai - Shanghai (Tower A) posted: Posted 22 Days Ago ### Senior Scientist, Analytical Development and Quality Control (Drug Product) - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: Not disclosed - Posted: 2026-05-13 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8546901002 - Excerpt: Senior Scientist, Analytical Development and Quality Control (Drug Product) Brisbane, CA Company Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Position Nurix Therapeutics seeks an experienced Senior Scientist to join the Analytical Development and Quality Control group. The Senior Scientist will be responsible for drug product (DP) analytical development, including method development, oversight of method validation at CDMOs, and lifecycle management in support of Nurix's oncology and inflammation & immunology (I&I) programs. This position provides technical oversight of analytical method development, validation, and testing conducted at external CDMO/CRO partners. The Senior Scientist will author analytical development reports and IND/IMPD/NDA sections and support late-phase tech transfer and validation activities. This role will also contribute to analytical development for new drug products and dosage forms. The Senior Scientist will work closely in cross-functional teams to ensure alignment and integration of analytical and QC strategies across development stages. The ideal candidate will have expertise in chromatographic and dissolution method development, stability ### Pharmaceutical Manufacturer Relations Executive - Humana Inc. - Location: Remote Nationwide (remote) - Salary: Not disclosed - Posted: 2026-06-10 - 401(k) match: listed (not source-backed) - Apply: https://humana.wd5.myworkdayjobs.com/CenterWell_External_Career_Site/job/Remote-Nationwide/Pharmaceutical-Manufacturer-Relations-Executive_R-419074 - Excerpt: Pharmaceutical Manufacturer Relations Executive Remote Nationwide posted: Posted 2 Days Ago ### Director, Health Economics & Outcomes Research (HEOR) - Vaxcyte Inc - Location: San Carlos, California, United States (unspecified) - Salary: $242K-$282K - Posted: 2026-03-09 - 401(k) match: listed (not source-backed) - Apply: https://boards.greenhouse.io/vaxcyte/jobs/5147570008?gh_jid=5147570008 - Excerpt: Director, Health Economics & Outcomes Research (HEOR) San Carlos, California, United States Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered. *AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary: Vaxcyte is seeking a Director, Health Economics & Outcomes Research (HEOR) to establish and lead the company's health economic strategy across the vaccine lifecycle, with initial focus on adult pneumococcal programs. This strategic leadership role will be responsible for developing and executing global health economic models to support payer ### Pharmaceutical Information Specialist - Merck & Co., Inc. - Location: CHN - Shanghai - Shanghai (Tower A) (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Tower-A/Pharmaceutical-Information-Specialist_R401276-1 - Excerpt: Pharmaceutical Information Specialist CHN - Shanghai - Shanghai (Tower A) posted: Posted 7 Days Ago ### Director, Pharmaceutical Analytical Sciences - Merck & Co., Inc. - Location: USA - New Jersey - Rahway (unspecified) - Salary: Not disclosed - Posted: 2026-05-14 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/USA---New-Jersey---Rahway/Director--Pharmaceutical-Analytical-Sciences_R396510-1 - Excerpt: Director, Pharmaceutical Analytical Sciences USA - New Jersey - Rahway posted: Posted 29 Days Ago ### Senior Manager, Indirect Procurement - Clinical - Vaxcyte Inc - Location: San Carlos, California, United States (unspecified) - Salary: $159K-$186K - Posted: 2026-04-22 - 401(k) match: listed (not source-backed) - Apply: https://boards.greenhouse.io/vaxcyte/jobs/5195377008?gh_jid=5195377008 - Excerpt: Senior Manager, Indirect Procurement - Clinical San Carlos, California, United States Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered. *AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary: This is an exciting opportunity to lead procurement support for clinical development programs, serving as a strategic business partner to the Clinical Operations Department, while maintaining the ability to flex across enterprise-wide procurement priorities as business needs evolve. This role sits within the centralized Procurement function in Finance and serves ### Sr. Pharmaceutical Info Specialist,AI - Merck & Co., Inc. - Location: CHN - Jiangsu - Suzhou (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Jiangsu---Suzhou/Sr-Pharmaceutical-Info-Specialist-AI_R393894-2 - Excerpt: Sr. Pharmaceutical Info Specialist,AI CHN - Jiangsu - Suzhou posted: Posted 30+ Days Ago ### Pharmaceutical Information Manager - Merck & Co., Inc. - Location: CHN - Shanghai - Shanghai (Trading) (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Trading/Pharmaceutical-Information-Manager_R401755-2 - Excerpt: Pharmaceutical Information Manager CHN - Shanghai - Shanghai (Trading) posted: Posted 8 Days Ago ### Medical Director, Drug Safety - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: Not disclosed - Posted: 2026-05-15 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8552951002 - Excerpt: Medical Director, Drug Safety Brisbane, CA Title: Medical Director, Drug Safety Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Position: As a Medical Director, Drug Safety you will play a key role in ensuring the safety of patients in Nurix's clinical trials. You will apply your clinical expertise to evaluate safety data, guide benefit-risk assessments and help shape the pharmacovigilance strategy for Nurix's emerging therapies. You will report to the VP of pharmacovigilance and work closely with colleagues in clinicaldevelopment, regulatory affairs, and clinical research to interpret emerging safety signals, support regulatory submissions, and maintain a strong safety framework during clinical development and transition into the post-marketing phase. Your insights will help inform critical decisions about patient safety, risk management, and the overall development strategy for our products. This role is well suited for a physician who enjoys working at the intersection of non-clinical data, clinical medicine, data interpretation, and drug development, and who wants to have a ### Sr. Pharmaceutical Info Specialist, Onco - Merck & Co., Inc. - Location: CHN - Shandong - Yantai (unspecified) - Salary: Not disclosed - Posted: 2026-06-01 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shandong---Yantai/Sr-Pharmaceutical-Info-Specialist--Onco_R398232-1 - Excerpt: Sr. Pharmaceutical Info Specialist, Onco CHN - Shandong - Yantai posted: Posted 11 Days Ago ### 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 ### VP, Medical Affairs – Hematology-Oncology - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-08 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8582375002 - Excerpt: VP, Medical Affairs – Hematology-Oncology Brisbane, CA Company Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Position Overview Nurix Therapeutics is seeking a Vice President, Medical Affairs, Hematology-Oncology to build, expand, and lead a best-in-class Medical Affairs organization supporting the company's transition from a clinical-stage biotechnology company toward commercialization as its hematology-oncology portfolio advances into late-stage clinical development. This executive will provide strategic and operational leadership across the full Medical Affairs function, including medical strategy, field medical, scientific communications, evidence generation, thought leader engagement, medical information, and launch readiness. The role will play a central role in shaping the scientific and medical strategy for Nurix's targeted protein degradation portfolio and helping define the company's external scientific leadership in hematologic malignancies. The role will be a key cross-functional partner to Clinical Development, Commercial, Market Access, Regulatory, Legal, and Compliance as Nurix plans and executes future commercialization activities. This leader will contribute broadly to portfolio strategy, lifecycle planning, and enterprise-level ### Pharmaceutical Production Lead - All Shifts - Medline Inc. - Location: Waukegan, Illinois (unspecified) - Salary: Not disclosed - Posted: 2026-05-14 - 401(k) match: listed (not source-backed) - Apply: https://medline.wd5.myworkdayjobs.com/Medline/job/Waukegan-Illinois/Pharmaceutical-Production-Lead---All-Shifts_R2605412 - Excerpt: Pharmaceutical Production Lead - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago ### Associate Director, Computer Systems Assurance (Quality) - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: $190K-$216K - Posted: 2026-05-05 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8535914002 - Excerpt: Associate Director, Computer Systems Assurance (Quality) Brisbane, CA Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Position The Senior Manager / Associate Director, Computer Systems Assurance (CSA) is an important technical and operational leader within the Nurix Quality Systems organization, responsible for owning and advancing Nurix's computer systems assurance program. As a virtual drug developer, Nurix operates through a lean internal infrastructure and relies on a curated ecosystem of Software-as-a-Service (SaaS) and cloud-hosted platforms to support GxP-regulated activities across clinical development, quality operations, manufacturing oversight, and regulatory submissions. This role will serve as the primary subject matter expert and program owner for all CSA and computerized system validation (CSV) activities at Nurix. Reporting to the Vice President / Senior Director, Quality Systems, this individual will establish and maintain Nurix's risk-based CSA framework aligned with current regulatory expectations, including the FDA's 2022 guidance on computer software assurance, GAMP 5 (2nd edition), and applicable 21 CFR Part 11 and Annex ### 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 ### Pharmaceutical Production Technician - All Shifts - Medline Inc. - Location: Waukegan, Illinois (unspecified) - Salary: Not disclosed - Posted: 2026-05-14 - 401(k) match: listed (not source-backed) - Apply: https://medline.wd5.myworkdayjobs.com/Medline/job/Waukegan-Illinois/Pharmaceutical-Production-Technician---All-Shifts_R2605411 - Excerpt: Pharmaceutical Production Technician - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago ### Pharmaceutical Product Operator - All Shifts - Medline Inc. - Location: Waukegan, Illinois (unspecified) - Salary: Not disclosed - Posted: 2026-05-14 - 401(k) match: listed (not source-backed) - Apply: https://medline.wd5.myworkdayjobs.com/Medline/job/Waukegan-Illinois/Pharmaceutical-Product-Operator_R2605410 - Excerpt: Pharmaceutical Product Operator - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago ### Vice President, Head of Alliance Management and Program Management ~ Onsite - Nurix Therapeutics Inc - Location: Brisbane, CA (onsite) - Salary: Not disclosed - Posted: 2026-05-07 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8540264002 - Excerpt: Vice President, Head of Alliance Management and Program Management ~ Onsite Brisbane, CA Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Vice President, Head of Alliance Management and Program Management Nurix Therapeutics is seeking an accomplished and strategic Vice President, Head of Alliance Management and Program Management to lead both our external collaborations with pharmaceutical partners and the internal coordination of our late stage hematology/oncology program. In addition to leading a high-impact alliance, this role will drive internal program management discipline, ensuring organizational awareness of program priorities, clear accountability for key workstreams, aligned roadmaps across functions, and transparent communication of status and risks to senior leadership. The ideal candidate is a dynamic leader who thrives in complexity, bridges science and business, and delivers executional excellence across partnerships and programs. Key Responsibilities - Alliance Leadership and Strategy - Serve as the primary point of contact between Nurix Therapeutics and its pharmaceutical partners, fostering a transparent, collaborative, and goal-oriented relationship. ### Manager/Senior Manager, Trial Operations - Xenon Pharmaceuticals - Location: Boston | [Hybrid] | Remote (hybrid) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://jobs.ashbyhq.com/xenon/b83ed917-f851-4a2a-bfed-8b2dd29babd3 - Excerpt: Manager/Senior Manager, Trial Operations Boston | [Hybrid] | Remote ### Asso. Pharmaceutical Information Manager, Onco - Merck & Co., Inc. - Location: CHN - Guangdong - Foshan (unspecified) - Salary: Not disclosed - Posted: 2026-05-28 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Guangdong---Foshan/Asso-Pharmaceutical-Information-Manager--Onco_R400857-1 - Excerpt: Asso. Pharmaceutical Information Manager, Onco CHN - Guangdong - Foshan posted: Posted 15 Days Ago ### Director, Medical Affairs - ORIC Pharmaceuticals - Location: South San Francisco, CA, United States | Remote (remote) - Salary: $220K-$275K - Posted: 2026-06-10 - Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990013504016--director-medical-affairs - Excerpt: Director, Medical Affairs South San Francisco, CA, United States | Remote Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . ORIC Pharmaceuticals is seeking a Director, Medical Affairs, as a member of the Global Medical Affairs (GMA) team based in ORIC's South San Francisco office. Reporting to the Head of Medical Affairs, this individual will be responsible for developing and executing the GMA strategy and tactical plans with a focus on launch readiness and life cycle management for therapies across prostate cancer, non-small cell lung cancer (NSCLC), and potentially other tumor types. The successful candidate will have a proven track record of developing and driving medical strategy for multiple assets with a focus on effectively analyzing and communicating key scientific data through publications, medical information, medical communications, congress activities as well as gathering insights through advisory boards, advocacy, and ### Senior Manager, Quality Operations - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: $138K-$156K - Posted: 2026-04-03 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8493600002 - Excerpt: Senior Manager, Quality Operations Brisbane, CA Senior Manager, Quality Operations Nurix Therapeutics is a clinical-stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation therapeutics. Leveraging our proprietary DELigase platform, we design small molecules that harness the body's own protein disposal system to selectively eliminate disease-causing proteins. Our pipeline spans oncology and immune-mediated diseases, and our team is united by a commitment to scientific excellence and meaningful impact for patients. We are a team of scientists, innovators, and problem-solvers committed to improving patient lives. We value integrity in everything we do - from the bench to the boardroom - and we foster an environment where every voice is heard and every contribution matters. Position The Senior Manager, Quality Operations is an important operational and technical contributor within the Nurix Quality organization, responsible for supporting the quality operations and GMP compliance activities that underpin Nurix's clinical development programs. This role will partner closely with CMC teams, CDMOs, and internal stakeholders to ensure quality oversight across drug manufacturing, laboratory operations, auditing, and inspection readiness. Reporting to the Senior Director, Quality, the Senior Manager will execute essential quality systems activities including deviation management, change control, CAPA, batch record review, and audit support. This individual will demonstrate strong independent judgment, meticulous attention to detail, and the ability to collaborate effectively across functions in a dynamic, early to late clinical-stage environment where quality and program timelines are closely intertwined Responsibilities Drug Manufacturing Quality Operations - Execute and support quality systems operations ### Werkstudent (m/w/d) Pharmaceutical Technical Solutions - Merck & Co., Inc. - Location: DEU - Niedersachsen - Friesoythe (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/DEU---Niedersachsen---Friesoythe/Werkstudent--m-w-d--Quality-Assurance-Systems_R384362 - Excerpt: Werkstudent (m/w/d) Pharmaceutical Technical Solutions DEU - Niedersachsen - Friesoythe posted: Posted 30+ Days Ago ### Principal, Volume Forecasting - Genedx Holdings CORP - Location: Remote (remote) - Salary: $150K-$170K - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://genedx.com/careers/openings?gh_jid=4681776005 - Excerpt: Principal, Volume Forecasting Remote GeneDx (Nasdaq: WGS) delivers personalized and actionable health insights to inform diagnosis, direct treatment, and improve drug discovery. The company is uniquely positioned to accelerate the use of genomic and large-scale clinical information to enable precision medicine as the standard of care. GeneDx is at the forefront of transforming healthcare through its industry-leading exome and genome testing and interpretation services, fueled by the world's largest, rare disease data sets. For more information, please visit www.genedx.com . Summary We are seeking a Principal, Volume Forecasting to own and advance GeneDx's end-to-end forecasting capability. This is a senior individual contributor role with high autonomy and broad cross-functional influence. You will build rigorous, data-driven models, drive full adoption of AI and automation tooling, lead forecasting cycles, and deliver the insights that shape strategic decisions across our diagnostics business - all with minimal leadership support in a fast-paced, high-growth organization. Job Responsibilities Own the design, build, and continuous improvement of driver-based volume forecast models integrating historical trends, pipeline data, seasonality, payer/channel mix, and market intelligence across all product lines, architected to scale with new market entries and test launches Select and apply appropriate statistical and machine learning forecasting methodologies (e.g., ARIMA, exponential smoothing, regression, ensemble/ML methods) based on data characteristics, forecast horizon, and business context Drive full adoption of AI and automation across the forecasting scope, from data ingestion and feature engineering through model training, validation, and reporting, and replace manual processes with scalable, reproducible pipelines Lead monthly, quarterly, and ### Scientist, Pharmaceutical Analytical Sciences - Merck & Co., Inc. - Location: USA - New Jersey - Rahway (unspecified) - Salary: Not disclosed - Posted: 2026-06-02 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/USA---New-Jersey---Rahway/Scientist--Pharmaceutical-Analytical-Sciences_R395348-2 - Excerpt: Scientist, Pharmaceutical Analytical Sciences USA - New Jersey - Rahway posted: Posted 10 Days Ago ### Sr. Pharmaceutical Info Specialist, ANA - Merck & Co., Inc. - Location: CHN - Shanghai - Shanghai (Tower A) (unspecified) - Salary: Not disclosed - Posted: 2026-06-02 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Tower-A/Sr-Pharmaceutical-Info-Specialist--ANA_R395198-1 - Excerpt: Sr. Pharmaceutical Info Specialist, ANA CHN - Shanghai - Shanghai (Tower A) posted: Posted 10 Days Ago ### Senior Director, Regulatory Affairs (Strategy, Hematology Oncology) - Nurix Therapeutics Inc - Location: Brisbane, California, United States (unspecified) - Salary: Not disclosed - Posted: 2026-05-09 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8542231002 - Excerpt: Senior Director, Regulatory Affairs (Strategy, Hematology Oncology) Brisbane, California, United States Position Title: Senior Director, Regulatory Affairs (Strategy, Hematology Oncology) Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Job Summary: Nurix Therapeutics, Inc. is seeking a Senior Director Regulatory Affairs (Strategy, Hematology Oncology) to join the Regulatory team. The successful candidate will be a core member of the Regulatory team and will be responsible for helping build and execute on global regulatory strategy, objectives, policies and programs pertaining to development and future marketing of products for guiding and executing upon regulatory strategy of compliant, high quality, nonclinical and clinical submissions and interactions in support of early development, registration and life cycle management activities. This includes supporting regulatory activities to enable clinical development plans and studies, working cross-functionally across the organization. Responsibilities: - Provides regulatory strategic direction and support for assigned global development programs/development program activities - Assists Sr. Regulatory Affairs staff with their development program activities and deliverables ### Manager, Quality Systems & Administration - Tonix Pharmaceuticals Holding Corp - Location: North Dartmouth, MA (unspecified) - Salary: $110K-$145K - Posted: 2026-04-13 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/tonixpharmaceuticals/jobs/4214661009 - Excerpt: Manager, Quality Systems & Administration North Dartmouth, MA Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix's CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit www.tonixpharma.com and follow the Company on LinkedIn and X . *Tonix's product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication. Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners. Position Overview: The Manager, Quality Systems ### Pharmaceutical Information Manager, Onco - Merck & Co., Inc. - Location: CHN - Beijing - Beijing (Oriental Towers) (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Beijing---Beijing-Oriental-Towers/Pharmaceutical-Information-Manager--Onco_R400628-2 - Excerpt: Pharmaceutical Information Manager, Onco CHN - Beijing - Beijing (Oriental Towers) posted: Posted 8 Days Ago ### Senior Associate Scientist (Contract), Drug Product Analytics - Vaxcyte Inc - Location: San Carlos, California, United States (unspecified) - Salary: $56-$62/hr - Posted: 2026-03-23 - 401(k) match: listed (not source-backed) - Apply: https://boards.greenhouse.io/vaxcyte/jobs/5154315008?gh_jid=5154315008 - Excerpt: Senior Associate Scientist (Contract), Drug Product Analytics San Carlos, California, United States Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered. *AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary: Vaxcyte is looking for an energetic and talented individual to join our Drug Product Development team. The candidate must have knowledge of and practical experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) using a variety of methods, especially immunoassays and multiplexed immunoassay formats. Experience in analyzing vaccine ### Asso. Pharmaceutical Information Manager - Merck & Co., Inc. - Location: CHN - Beijing - Beijing (Oriental Towers) (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Beijing---Beijing-Oriental-Towers/Asso-Pharmaceutical-Information-Manager_R399328-1 - Excerpt: Asso. Pharmaceutical Information Manager CHN - Beijing - Beijing (Oriental Towers) posted: Posted 8 Days Ago ### Pharmaceutical Technician (WDA) - Merck & Co., Inc. - Location: SGP - Singapore - Singapore (70 Tuas West Dr) (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/SGP---Singapore---Singapore-70-Tuas-West-Dr/Pharmaceutical-Technician--WDA-_R378025 - Excerpt: Pharmaceutical Technician (WDA) SGP - Singapore - Singapore (70 Tuas West Dr) posted: Posted Yesterday ### Senior Manager, Pharmacovigilance - ORIC Pharmaceuticals - Location: San Diego, CA, United States | Remote (remote) - Salary: $150K-$180K - Posted: 2026-06-10 - Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990011886996-senior-manager-pharmacovigilance - Excerpt: Senior Manager, Pharmacovigilance San Diego, CA, United States | Remote Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . The Senior Manager of Pharmacovigilance will be responsible for the execution of global pharmacovigilance activities supporting late-stage clinical development and preparation for first commercial launch of small-molecule oncology products in lung and prostate cancer. This role will ensure compliance with global safety regulations and will work closely with cross-functional partners to ensure individual case safety report (ICSR) processing, Health Authority submissions, and post-marketing safety readiness. This is a hands-on role well suited for a biotech environment requiring both operational excellence and cross-functional collaboration. Job Description: Global Drug Safety & Pharmacovigilance Operations Manage end-to-end pharmacovigilance activities for clinical trials and post-approval oncology products In partnership with Clinical Research Organizations (CROs), oversee intake, assessment, processing, medical review, and reporting of ICSRs from ### Pharmaceutical Technician (WDA) - Merck & Co., Inc. - Location: SGP - Singapore - Singapore (70 Tuas West Dr) (unspecified) - Salary: Not disclosed - Posted: 2026-06-02 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/SGP---Singapore---Singapore-70-Tuas-West-Dr/Pharmaceutical-Technician--WDA-_R392851 - Excerpt: Pharmaceutical Technician (WDA) SGP - Singapore - Singapore (70 Tuas West Dr) posted: Posted 10 Days Ago ### Senior Director, Quality - ORIC Pharmaceuticals - Location: San Diego, CA, United States (unspecified) - Salary: $220K-$270K - Posted: 2026-06-10 - Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990011995852-senior-director-quality- - Excerpt: Senior Director, Quality San Diego, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . Reporting to the Senior Vice President of Quality, the Sr. Director of Quality will lead provide quality oversight of clinical development and manufacturing programs. This individual will lead the Chemistry, Manufacturing, and Controls (CMC) QA team and provide end-to-end development to manufacturing support for clinical stage programs and will develop systems to commercialize late-stage assets. This position will design, develop, and implement clinical and commercial quality strategies to ensure appropriate compliance to applicable regulatory regulations. The successful candidate will work closely with Technical Operations, Regulatory Affairs, and third-party Contract Development and Manufacturing Organizations (CDMOs) and will be responsible for all levels of studies, ranging from simple to complex and requires an in-depth understanding of GMPs, global Health Authority requirements, program management, quality ### AIRx Director, Computational & AI Biologics Design Lead - Takeda Pharmaceutical Company Limited - Location: Boston, MA (unspecified) - Salary: Not disclosed - Posted: 2026-06-09 - 401(k) match: listed (not source-backed) - Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Boston-MA/AIRx-Director--Computational---AI-Biologics-Design-Lead_R0181773 - Excerpt: AIRx Director, Computational & AI Biologics Design Lead Boston, MA posted: Posted 3 Days Ago ### Operator – Start-up of a New Pharmaceutical Facility - Merck & Co., Inc. - Location: NLD - North Brabant - Boxmeer (unspecified) - Salary: Not disclosed - Posted: 2026-06-03 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/NLD---North-Brabant---Boxmeer/Operator---Nieuwe-Farmaceutische-Fabriek_R393536-1 - Excerpt: Operator – Start-up of a New Pharmaceutical Facility NLD - North Brabant - Boxmeer posted: Posted 9 Days Ago ### Medical Science Liaison (MSL) - West - Syndax Pharmaceuticals Inc - Location: West Coast (unspecified) - Salary: $235K-$260K - Posted: 2026-05-26 - 401(k) match: listed (not source-backed) - Apply: https://syndax.com/join-us/careers/?gh_jid=6006343004 - Excerpt: Medical Science Liaison (MSL) - West West Coast Syndax Pharmaceuticals is looking for a Medical Science Liaison (MSL ) - West At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies. We are interested in territory coverage in the following states: California, Washington, Oregon, Montana, Idaho Nevada, Utah, Arizona, Wyoming, Colorado, New Mexico, Alaska, Hawaii The Role: Syndax is searching for a Medical Science Liaison (MSL) in our West region responsible for identifying, developing, and managing relationships with current and future hematology/oncology Key Opinion Leaders (KOLs) and other health care providers in academic and community practices. The MSL will be a key member of the Field Medical Affairs team at Syndax. This position will be the primary communicator of Syndax science and will be responsible for executing the national medical affairs plan within their assigned territory. Key Responsibilities: KOL & Relationship Building - Develop and foster strong scientific relationships with Key Opinion Leaders (KOLs), disease experts, and other health care providers (HCPs). - Engage in peer-to-peer scientific exchange of complex clinical and scientific data and information. - Act as a primary point of contact to address scientific inquiries and deliver presentations on disease state, mechanisms of action, and clinical data, and serve as the scientific expert in support of Syndax therapeutic areas of interest. - Identify and evaluate Key Opinion Leaders (KOLs) and profile ### Sr. Pharmaceutical Info Specialist，Retail - Merck & Co., Inc. - Location: CHN - Xinjiang - Urumuqi (Tianshan District) (unspecified) - Salary: Not disclosed - Posted: 2026-05-13 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Xinjiang---Urumuqi-Tianshan-District/Sr-Pharmaceutical-Info-Specialist-Retail_R398280-1 - Excerpt: Sr. Pharmaceutical Info Specialist，Retail CHN - Xinjiang - Urumuqi (Tianshan District) posted: Posted 30 Days Ago ### Manager, Market Intelligence and Strategy - Entrada Therapeutics Inc - Location: Boston, MA (unspecified) - Salary: $127K-$166K - Posted: 2026-05-08 - Parental leave: 0 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/entradatherapeutics/jobs/5132958007 - Excerpt: Manager, Market Intelligence and Strategy Boston, MA The Organization What's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1). 2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670). We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. The Perfect Addition to Our Team You are interested in working at the intersection of life sciences and business. You want to join a high ### Représentant(e) en ventes pharmaceutiques / Pharmaceutical Sales Representative - Merck & Co., Inc. - Location: CAN - Quebec - Quebec City (unspecified) - Salary: Not disclosed - Posted: 2026-06-03 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CAN---Quebec---Quebec-City/Reprsentant-e--en-ventes-pharmaceutiques---Pharmaceutical-Sales-Representative_R401727-1 - Excerpt: Représentant(e) en ventes pharmaceutiques / Pharmaceutical Sales Representative CAN - Quebec - Quebec City posted: Posted 9 Days Ago ### Senior Operator – Start-up of a New Pharmaceutical Facility - Merck & Co., Inc. - Location: NLD - North Brabant - Boxmeer (unspecified) - Salary: Not disclosed - Posted: 2026-06-03 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/NLD---North-Brabant---Boxmeer/Senior-Operator---Start-up-of-a-New-Pharmaceutical-Facility_R401808 - Excerpt: Senior Operator – Start-up of a New Pharmaceutical Facility NLD - North Brabant - Boxmeer posted: Posted 9 Days Ago ### Medical Director/Senior Medical Director, Clinical Development (Prostate) - ORIC Pharmaceuticals - Location: San Diego, CA, United States (unspecified) - Salary: $270K-$320K - Posted: 2026-06-10 - Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990013417826-medical-director-senior-medical-director-clinical-development-prostate- - Excerpt: Medical Director/Senior Medical Director, Clinical Development (Prostate) San Diego, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat, an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . We are seeking an experienced oncology physician to serve as a Medical Director or Senior Medical Director at ORIC Pharmaceuticals. This role provides medical leadership across one or more clinical development programs, with a primary focus on late-stage (registration-enabling) clinical trials. The position plays a critical role in shaping clinical strategy, ensuring scientific rigor, guiding regulatory interactions, and advancing programs from study design through regulatory submission. The Medical Director will work in close partnership with cross-functional teams including Clinical Operations, Regulatory Affairs, Biostatistics, Safety/Pharmacovigilance, Translational Medicine, and Medical Affairs. The role requires strong strategic thinking, hands-on execution, and the ability to lead effectively in a fast-paced biotech environment. Job Description: Clinical and Medical Leadership Serve as the medical lead ### International Clinical Analyst - Genedx Holdings CORP - Location: Remote (remote) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://genedx.com/careers/openings?gh_jid=4704807005 - Excerpt: International Clinical Analyst Remote GeneDx (Nasdaq: WGS) delivers personalized and actionable health insights to inform diagnosis, direct treatment, and improve drug discovery. The company is uniquely positioned to accelerate the use of genomic and large-scale clinical information to enable precision medicine as the standard of care. GeneDx is at the forefront of transforming healthcare through its industry-leading exome and genome testing and interpretation services, fueled by the world's largest, rare disease data sets. For more information, please visit www.genedx.com . Summary The Clinical Analyst II (AMBGG certified) serves as a key contributor to the interpretation of genetic findings, supports accurate diagnosis and case resolution through exome and genome sequencing workflows. This mid-level role builds on foundational clinical analysis competencies by performing independent case reviews with minimal supervision. Job Responsibilities Independently perform clinical data analysis and case management to support accurate interpretation of genetic findings, including reanalysis activities. Establish phenotype-genotype correlations across a wide range of genetic disorders using internal resources and professional tools. Investigates and interprets complex clinical features of genetic conditions; documents evidence and rationale for variant classification in a clear, standardized format. Meets or exceeds productivity and error standards as assigned by team lead. Perform clinical analysis at moderate case rate. Perform other duties as assigned to advance team objectives. People Manager No Education, Experience, and Skills PhD in Biology, Genetics or related field, MD or DO with more than 2 years directly relevant experience in clinical diagnostics (including fellowship) Excellent verbal and written communication skills Demonstrated computer ### Improvement Officer - Start-up of a new pharmaceutical facility - Merck & Co., Inc. - Location: NLD - North Brabant - Boxmeer (unspecified) - Salary: Not disclosed - Posted: 2026-06-03 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/NLD---North-Brabant---Boxmeer/Improvement-Officer---Start-up-of-a-new-pharmaceutical-facility_R401802-2 - Excerpt: Improvement Officer - Start-up of a new pharmaceutical facility NLD - North Brabant - Boxmeer posted: Posted 9 Days Ago ### Senior Manager, Boomi Developer - Syndax Pharmaceuticals Inc - Location: Boston, MA (unspecified) - Salary: $160K-$175K - Posted: 2026-05-29 - 401(k) match: listed (not source-backed) - Apply: https://syndax.com/join-us/careers/?gh_jid=6009464004 - Excerpt: Senior Manager, Boomi Developer Boston, MA Syndax Pharmaceuticals is looking for a Senior Manager, Boomi Developer At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies. Please note, the ideal candidate for this role will be located in the Northeast. The Role: Syndax Pharmaceuticals is seeking a highly motivated Senior Manager, Boomi Developer to design, build, and support integrations across our enterprise application ecosystem. This role is primarily focused on Boomi AtomSphere development, including integration workflows and Master Data Hub (MDH), while also supporting and enhancing critical employee lifecycle integrations (onboarding and offboarding). The ideal candidate is a proactive, adaptable self-starter who thrives in a fast-paced, small biotech environment. This individual will take ownership across multiple areas, quickly learn new systems, and contribute beyond their core expertise. Experience with the Boomi platform and enterprise applications is essential. This is an exciting opportunity to help scale integration capabilities in a growing commercial-stage biotechnology organization, enabling efficient and reliable data flow across enterprise systems. Key Responsibilities: - Design, develop, and maintain integrations using Boomi AtomSphere - Build and support data synchronization and governance processes within Boomi Master Data Hub (MDH) - Own the full integration lifecycle, including: - Requirements gathering - Solution design and development - Testing and deployment - Monitoring and support - Ensure data accuracy and consistency across employee lifecycle events (hire, transfer, termination) ### Pharmaceutical Sales Representative/ Représentant(e) en ventes pharmaceutiques (Alberta) - Merck & Co., Inc. - Location: 3 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-08 - 401(k) match: listed (not source-backed) - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CAN---Quebec---Kirkland-16750-Transcanada/Pharmaceutical-Sales-Representative---Reprsentant-e--en-ventes-pharmaceutiques--Alberta-_R401426-1 - Excerpt: Pharmaceutical Sales Representative/ Représentant(e) en ventes pharmaceutiques (Alberta) 3 Locations posted: Posted 4 Days Ago ### Sr. Director, Head of Regulatory & Medical Writing - Nurix Therapeutics Inc - Location: Brisbane, California, United States (unspecified) - Salary: $254K-$289K - Posted: 2026-05-09 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8542236002 - Excerpt: Sr. Director, Head of Regulatory & Medical Writing Brisbane, California, United States Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Job Summary: As a key member of the cross-functional Development Team responsible for providing regulatory writing expertise and leadership to formulate the writing strategy for key regulatory documents for submission. The Sr. Director, Head of Regulatory & Medical Writing will be responsible for providing guidance to the medical and or regulatory writing group (contractors and internal writers) assigned to deliverables and ensuring appropriate work allocation and document preparation.; will also provide review and substantive editing of documents to ensure delivery of high-quality documents. This individual will work effectively with many other functional groups, including with Clinical Scientist(s), Medical Monitors, Regulatory and other functions as applicable, and collaborate with clinical medical writing as applicable to ensure scientific excellence in the execution of clinical trials. The Head of Regulatory Writing will build a medical writing group internally when appropriate. Reporting ### Pharmaceutical Purchasing and Inventory Coordinator - Elevance Health, Inc. - Location: TX-PLANO, 3033 W PRESIDENT GEORGE BUSH HWY, STE 100 (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - 401(k) match: listed (not source-backed) - Apply: https://elevancehealth.wd1.myworkdayjobs.com/ANT/job/TX-PLANO-3033-W-PRESIDENT-GEORGE-BUSH-HWY-STE-100/Purchasing-Coordinator---Rx--US-_JR193456 - Excerpt: Pharmaceutical Purchasing and Inventory Coordinator TX-PLANO, 3033 W PRESIDENT GEORGE BUSH HWY, STE 100 posted: Posted 7 Days Ago ### Vice President, Pharmaceutical Development - Kymera Therapeutics Inc - Location: Watertown, MA (unspecified) - Salary: $315K-$395K - Posted: 2026-05-26 - 401(k) match: listed (not source-backed) - Apply: https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7748334003#open-positions - Excerpt: Vice President, Pharmaceutical Development Watertown, MA Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston's top workplaces for the past several years. For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn . How we work: - PIONEER : We are courageous, resilient and rigorous in our mission to improve patients' lives through our revolutionary degrader medicines. - COLLABORATE : We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine. - BELONG : We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard. How you'll make an impact: - Define and lead the company's pharmaceutical development strategy across the portfolio, ensuring alignment with corporate priorities and development timelines - Provide strategic leadership for preformulation, biopharmaceutics, and formulation development activities supporting discovery, preclinical, and clinical-stage programs - Champion innovation in formulation sciences and enabling technologies to ### Technician, Pharmaceutical - AbbVie Inc. - Location: Sligo, SO, Ireland (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/3743990013577016-technician-pharmaceutical - Excerpt: Technician, Pharmaceutical Sligo, SO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: We are recruiting a Pharmaceutical Technician to join our team on site in Manorhamilton Road, Sligo on a 12 month fixed-term contract. This role is rotational shift work. In your role as Pharmaceutical Technician you will be responsible for producing drug product materials as per organizational needs in line with all relevant compliance requirements. This person will operate as a team member in a pharmaceutical processing facility in line with all regulatory and organizational requirements. A snapshot of your key responsibilities as a Pharmaceutical Technician would be: Pharmaceutical processing activities in our manufacturing building and support locations. Team co-ordination to maximise the effectiveness of the team members. Documentation of all activities in line with cGMP requirements. Cross training within the team and training of new team members. Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems. Execution of commissioning and validation protocols on an ongoing basis. Maintaining the overall cGMP of the pharmaceutical processing areas. Adheres ### VP, Patient Advocacy - BioMarin Pharmaceutical - Location: Location not specified (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - 401(k) match: listed (not source-backed) - Apply: https://jobs.jobvite.com/biomarin/job/ocMOzfw5 - Excerpt: VP, Patient Advocacy VP, Patient Advocacy ### Senior Director of Translational Sciences - Lb Pharmaceuticals Inc - Location: Location not specified (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://lbpharmaceuticals.bamboohr.com/careers/35 - Excerpt: Senior Director of Translational Sciences Senior Director of Translational Sciences ### Director, Pharmaceutical Development - Fulcrum Therapeutics INC - Location: Cambridge, MA (unspecified) - Salary: $240K-$240K - Posted: 2026-04-09 - 401(k) match: listed (not source-backed) - Apply: https://boards.greenhouse.io/fulcrumtherapeutics/jobs/8498670002?gh_jid=8498670002 - Excerpt: Director, Pharmaceutical Development Cambridge, MA Company Overview Fulcrum Therapeutics, Inc. (“Fulcrum”) [NASDAQ: FULC] is a clinical-stage biopharmaceutical company focused on developing small molecules to improve the lives of patients with genetically defined rare diseases. Fulcrum is deeply committed to bringing hope and new options to patients suffering from rare hematologic disorders and is developing a pipeline of clinical and preclinical assets. Fulcrum's lead clinical asset is pociredir, a first-in-class small molecule designed to increase the expression of fetal hemoglobin for the treatment of sickle cell disease and other hemoglobinopathies. We are working to expand our portfolio of clinical-stage assets and seek a driven and strategic leader to head our Pharmaceutical Development function. Description Reporting to the Head of Technical Operations, the Director of Pharmaceutical Development will lead all drug product development activities including technical, managerial, and budgetary aspects. This includes formulation development, manufacture of clinical trial material, process optimization, scale-up, and validation. The successful candidate will lead, plan and manage the technical and business-related activities associated with drug product development and manufacturing at contract development and manufacturing vendors for all dosage form programs. Key Responsibilities Lead all strategic and tactical aspects of drug product development at Fulcrum Design and execute pharmaceutical product development plans for all development programs in accordance with corporate goals Collaborate with colleagues in Drug Substance, Analytical, ClinOps, QA, and Reg CMC to ensure plans are cross-functional, phase-appropriate, and on time Lead pharmaceutical development for the pociredir program, including CTM for pivotal clinical studies, pre-validation studies, validation ### Senior Manager, Regulatory Operations - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: Not disclosed - Posted: 2026-04-01 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8486138002 - Excerpt: Senior Manager, Regulatory Operations Brisbane, CA Company: Nurix Therapeutics is a biopharmaceutical company focused on the discovery, development and commercialization of small molecule therapies designed to modulate cellular protein levels as a novel treatment approach for cancer and immune disorders. Leveraging Nurix's extensive expertise in E3 ligases together with its proprietary DNA-encoded libraries, Nurix has built DELigase, an integrated discovery platform to identify and advance novel drug candidates targeting E3 ligases, a broad class of enzymes that can modulate proteins within the cell. Nurix's drug discovery approach is to either harness or inhibit the natural function of E3 ligases within the ubiquitin proteasome system to selectively decrease or increase cellular protein levels. Nurix's wholly owned pipeline comprises targeted protein degraders of Bruton's tyrosine kinase (BTK), a B-cell signaling protein, and an inhibitor of Casitas B-lineage lymphoma proto-oncogene-B (CBL-B), an E3 ligase that regulates T cell activation. Nurix is also progressing multiple programs through partnership, including an IRAK4 degrader in Phase 1 in partnership with Gilead and a STAT6 degrader in IND enabling studies with Sanofi. Multiple additional wholly owned and partnered programs are at various stages of preclinical development. Position: Reporting to the Director, Regulatory Affairs Project Management and Operations, the Senior Manager, Regulatory Operations provides key support to the Nurix Regulatory Affairs department. This position has responsibility for entry-level coordination, review, assembly and archival of regulatory submissions in Veeva RIMS and documents for health authorities (US FDA and global equivalents). The Senior Manager, Regulatory Operations will provide support for ### Pharmaceutical Technician - 6 Month Contract - 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/3743990012973717-pharmaceutical-technician-6-month-contract - Excerpt: Pharmaceutical Technician - 6 Month Contract Sligo, SO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: We are recruiting a Pharmaceutical Technician to join our team on site in Manorhamilton Road, Sligo on a 6 month fixed-term contract. This role is rotational shift work. In your role as Pharmaceutical Technician you will be responsible for producing drug product materials as per organizational needs in line with all relevant compliance requirements. This person will operate as a team member in a pharmaceutical processing facility in line with all regulatory and organizational requirements. A snapshot of your key responsibilities as a Pharmaceutical Technician would be: Pharmaceutical processing activities in our manufacturing building and support locations. Team co-ordination to maximise the effectiveness of the team members. Documentation of all activities in line with cGMP requirements. Cross training within the team and training of new team members. Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems. Execution of commissioning and validation protocols on an ongoing basis. Maintaining the overall cGMP of the ### Senior Director, Marketing - Olema Pharmaceuticals - Location: San Francisco, California (unspecified) - Salary: $250K-$285K - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/olema/jobs/5480105004 - Excerpt: Senior Director, Marketing San Francisco, California Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential. Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you're ready to join us at the edge of something unstoppable, let's make a profound impact together for our patients, for your career, for what's beyond . You can view our latest corporate deck and other presentations here . About the Role >>> Senior Director, Marketing As the Senior Director, Marketing you will design and execute the Commercial roadmap that enables the successful potential U.S. launch of palazestrant, Olema's lead program currently in Phase 3 for ER+ HER2- metastatic breast cancer. The ideal candidate will have experience in the commercialization of oral oncology therapies in breast cancer and a track record of leading successful oncology drug launches in the US. This role is based out of our San Francisco office and will require travel as needed. Your work will primarily encompass: Building the strategic marketing plan and leading launch readiness initiatives (branding, positioning, messaging platform, story flow and creative imagery) ### Director, Clinical Operations - Oruka Therapeutics Inc - Location: Waltham, Massachusetts, United States (unspecified) - Salary: $213K-$240K - Posted: 2026-05-29 - Apply: https://job-boards.greenhouse.io/oruka/jobs/5236048008 - Excerpt: Director, Clinical Operations Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Director, Clinical Operations Location: Waltham, MA Hybrid - onsite 3 days/week required Reports To : Vice President, Clinical Operations Role Overview: We are seeking an exceptionally nimble and flexible Director of Clinical Operations who has a track record of achievement across all aspects of trial setup and execution in a fast paced small biotech with limited infrastructure and resources. The individual will successfully lead and optimize activity across multiple studies for Oruka Therapeutics. This critical role demands a strategic leader who possesses a keen ability to "zoom in" on intricate operational details ### Director of Project Management-Clinical - Lb Pharmaceuticals Inc - Location: Location not specified (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://lbpharmaceuticals.bamboohr.com/careers/37 - Excerpt: Director of Project Management-Clinical Director of Project Management-Clinical ### Director, Health Systems (Northeast) - Genedx Holdings CORP - Location: Remote (remote) - Salary: $170K-$190K - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://genedx.com/careers/openings?gh_jid=4662279005 - Excerpt: Director, Health Systems (Northeast) Remote GeneDx (Nasdaq: WGS) delivers personalized and actionable health insights to inform diagnosis, direct treatment, and improve drug discovery. The company is uniquely positioned to accelerate the use of genomic and large-scale clinical information to enable precision medicine as the standard of care. GeneDx is at the forefront of transforming healthcare through its industry-leading exome and genome testing and interpretation services, fueled by the world's largest, rare disease data sets. For more information, please visit www.genedx.com . Summary GeneDx is seeking a high-performing, strategically minded Director to drive growth within assigned hospitals, IDNs and integrated care networks. This role is ideal for someone with experience in hospital-based sales or genomics, who excels at consultative selling, navigating complex hospital environments, and promoting rapid adoption of genomic testing. This role reports to the VP of Health Systems. The Director plays a vital role in driving revenue growth and forging strategic partnerships within hospital, IDNs and integrated care networks. This position focuses on building and nurturing relationships with key stakeholders, including C-suite executives, senior management, physicians, laboratory and IT operations teams, and department heads. The aim is to promote the adoption of enterprise-wide solutions that enhance operational efficiency and improve patient care outcomes. The role involves strategic planning, business development, and delivering high-quality services aligned with the hospital's mission and objectives. Territory - Northeast Travel as needed, including some weekends, evenings, or overnights for conferences, meetings, or special events. Expectation is up to 60% travel as required. Job Responsibilities ### Vice President, Portfolio and Program Strategy - Lb Pharmaceuticals Inc - Location: Location not specified (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://lbpharmaceuticals.bamboohr.com/careers/31 - Excerpt: Vice President, Portfolio and Program Strategy Vice President, Portfolio and Program Strategy ### Manager, Analytical Development and Quality Control (Brisbane, CA) - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: $147K-$171K - Posted: 2026-05-20 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8553686002 - Excerpt: Manager, Analytical Development and Quality Control (Brisbane, CA) Brisbane, CA Company Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Position The Manager, Analytical Development and Quality Control provides strategic and technical leadership for analytical CMC activities across multiple programs, with a strong emphasis on technology transfer and knowledge management. This role ensures successful transfer of analytical methods and associated knowledge to internal teams and external stakeholders, enabling consistent execution across development and manufacturing sites. The position requires deep expertise in analytical method development, validation, transfer, and lifecycle management in alignment with ICH guidelines, along with the ability to interpret data from a range of analytical techniques to support sound technical decision-making. In addition, this role is responsible for establishing and clearly communicating analytical control strategies across cross-functional teams, ensuring alignment and scientific rigor. The Manager drives robust knowledge management practices through high-quality technical writing, documentation, and data governance, including authoring and reviewing validation, transfer, and investigation reports. Strong ### MES Engineer (Night Shift) - Genentech, Inc. - Location: Hillsboro, Oregon, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-05-20 - 401(k) match: listed (not source-backed) - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/Hillsboro/MES-Engineer--Night-Shift-_202601-102416-1/apply - Excerpt: MES Engineer (Night Shift) Hillsboro, Oregon, United States of America Embrace the role of an MES Engineer (Night Shift) and play a pivotal role in advancing digital manufacturing for a leading pharmaceutical company. Leverage your expertise in MES, GMP, and automation to support critical operations, drive process improvements, and ensure quality in a dynamic, automated environment. Shape the future of pharmaceutical manufacturing with us! ### Senior Scientist, Analytical Sciences - ORIC Pharmaceuticals - Location: South San Francisco, CA, United States (unspecified) - Salary: $150K-$180K - Posted: 2026-06-10 - Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990011640247-senior-scientist-analytical-sciences - Excerpt: Senior Scientist, Analytical Sciences South San Francisco, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . We are seeking a lab-based, highly motivated Senior Scientist in Analytical Sciences. The candidate will be part of cross-functional teams providing analytical leadership on projects, work closely on a shared mission to bring new therapeutics to cancer patients. The successful candidate will report to the Sr. Director of Analytical Sciences Job Description: Independently lead analytical development and product characterization activities for our drug development portfolios. Provide oversight, technical guidance and tactical direction for analytical method development, transfer, validation, release, and stability testing activities at CDMOs. Function as a subject matter expert for in-depth physical/ chemical characterization of NCEs at CROs. Independently conceptualize, design, and conduct experiments; interpret and present data and conclusions to various audience, including senior leadership. Expected to ### Director of Clinical Operations, Phase I Enabling Studies - Lb Pharmaceuticals Inc - Location: Location not specified (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://lbpharmaceuticals.bamboohr.com/careers/27 - Excerpt: Director of Clinical Operations, Phase I Enabling Studies Director of Clinical Operations, Phase I Enabling Studies ### Senior Manager, Supply Chain Planner - Vaxcyte Inc - Location: San Carlos, California, United States (unspecified) - Salary: $176K-$205K - Posted: 2026-04-16 - 401(k) match: listed (not source-backed) - Apply: https://boards.greenhouse.io/vaxcyte/jobs/5188916008?gh_jid=5188916008 - Excerpt: Senior Manager, Supply Chain Planner San Carlos, California, United States Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered. *AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary: Vaxcyte is seeking a strategic and execution-focused Senior Manager, Supply Chain Planner to join our Supply Chain Planning Team. This role is responsible for leading end-to-end supply planning across clinical and commercial programs, including demand and supply planning, capacity management, inventory strategy, and scenario analysis. The ideal candidate brings deep experience ### Pharmaceutical Technician II - Thermo Fisher Scientific - Location: Singapore, Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://thermofisher.wd5.myworkdayjobs.com/ThermoFisherCareers/job/Singapore-Singapore/Pharmaceutical-Technician-II_R-01354187/apply - Excerpt: Pharmaceutical Technician II Singapore, Singapore Embrace the role of a Pharmaceutical Technician II and play a vital role in sterile pharmaceutical production. Operate advanced equipment, ensure GMP compliance, and support quality manufacturing processes. If you have hands-on experience in pharmaceutical manufacturing and a passion for safety and precision, this is your opportunity to make an impact. ### Thought Leader Liaison (TLL), West Region - Tonix Pharmaceuticals Holding Corp - Location: United States (unspecified) - Salary: $130K-$200K - Posted: 2026-02-12 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/tonixpharmaceuticals/jobs/4130652009 - Excerpt: Thought Leader Liaison (TLL), West Region United States Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix's CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit www.tonixpharma.com and follow the Company on LinkedIn and X . *Tonix's product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication. Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners. Position Overview The Associate Director, Thought ### FSP SCRA I（Changsha） - Fortrea Holdings Inc - Location: Shanghai, China (unspecified) - Salary: Not disclosed - Posted: 2024-12-18 - 401(k) match: listed (not source-backed) - Apply: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Shanghai/FSP-SCRA-I-Changsha-_2447386/apply - Excerpt: FSP SCRA I（Changsha） Shanghai, China As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and med... ### Senior Medical Director, Asset Lead – Oncology (Neuroendocrine Tumors / Carcinoid Syndrome) - Crinetics Pharmaceuticals INC - Location: Remote (remote) - Salary: $293K-$366K - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/Remote/Sr-Medical-Director--Carcinoid-Syndrome-Oncology-Asset-Lead_JR000540 - Excerpt: Senior Medical Director, Asset Lead – Oncology (Neuroendocrine Tumors / Carcinoid Syndrome) Remote Crinetics is a pharmaceutical company based in San Diego, California that develops much-needed therapies for people with rare endocrine diseases. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and robust pipeline across preclinical and clinical development. We are driven by science with a patient-centric and team-oriented culture. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Come join our team as we transform the lives of others. POSITION SUMMARY: Crinetics is seeking an experienced oncology Medical Affairs leader to serve as Senior Medical Director, Asset Lead - Oncology (Neuroendocrine Tumors / Carcinoid Syndrome), reporting to the Executive Director, Medical Affairs. This role will provide Medical Affairs leadership for a complex oncology program within the Neuroendocrine Tumor (NET) landscape, requiring deep expertise in oncology clinical development, competitive data interpretation, and cross functional medical strategy. This individual will be responsible for shaping and executing Medical Affairs strategy across evidence generation, scientific exchange, and KOL engagement, ensuring alignment with Clinical Development, Regulatory, Commercial, Market Access, Compliance, and Legal functions. The role demands strong scientific credibility in oncology, the ability to interpret and translate complex oncology data, and comfort ### Pharmaceutical Technician II - Thermo Fisher Scientific - Location: Singapore, Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://thermofisher.wd5.myworkdayjobs.com/ThermoFisherCareers/job/Singapore-Singapore/Pharmaceutical-Technician-II_R-01349946-1/apply - Excerpt: Pharmaceutical Technician II Singapore, Singapore Embrace the role of a Pharmaceutical Technician II and play a vital role in sterile pharmaceutical production. Operate advanced equipment, ensure GMP compliance, and support quality manufacturing processes. Ideal for candidates with 1-5 years' experience in pharma, this role offers hands-on work in a dynamic, safety-focused environment. Grow your career in pharmaceutical manufacturing today! ### Apprentice - Visual Design - Fortrea Holdings Inc - Location: BANGALORE, Karnātaka, India (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - 401(k) match: listed (not source-backed) - Apply: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Bangalore/Apprentice---Visual-Design_263011/apply - Excerpt: Apprentice - Visual Design BANGALORE, Karnātaka, India As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medi... ### Executive Director, AIRx Program Lead: Biologics - Takeda Pharmaceutical Company Limited - Location: Boston, MA (unspecified) - Salary: Not disclosed - Posted: 2026-05-31 - 401(k) match: listed (not source-backed) - Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Boston-MA/Executive-Director--AIRx-Program-Lead--Biologics_R0181169 - Excerpt: Executive Director, AIRx Program Lead: Biologics Boston, MA posted: Posted 12 Days Ago ### Apprentice - Employer Branding - Fortrea Holdings Inc - Location: BANGALORE, Karnātaka, India (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - 401(k) match: listed (not source-backed) - Apply: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Bangalore/Apprentice---Employer-Branding_263009/apply - Excerpt: Apprentice - Employer Branding BANGALORE, Karnātaka, India As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medi... ### Head of Product - Sully.AI - Location: US - Bay Area (unspecified) - Salary: Not disclosed - Posted: 2026-02-26 - Apply: https://jobs.ashbyhq.com/sully-ai/7d12f693-a3bf-4010-b22e-7ba0d09acf01 - Excerpt: Head of Product US - Bay Area About Us At Sully.ai , We're Building the Most Impactful Healthcare Company on Earth We believe that access to a great doctor is a basic human right. Today, that's not a reality. Delays, misdiagnoses, administrative chaos, and burnout plague the system. Our Mission One Human, One Doctor . We enable our customers to staff 30% of their workforce with AI by creating a shared agent architecture for scale and efficiency. All powered by our own patented, world-class models and deployed in real-world care. About the Role - We're hiring a Head of Product to own a specific Agent to execute Sully.ai 's product roadmap end-to-end, aligning product strategy with our mission and growth goals. You'll lead discovery, design, and delivery across the full product lifecycle-partnering closely with Engineering, Data Science, Sales, and Marketing to translate customer feedback into high-impact features that solve critical healthcare challenges. Key Responsibilities - Own a specific Agent to execute Sully.ai 's product roadmap, aligning with mission & growth goals. - Lead discovery, design, and delivery of features that solve critical healthcare challenges. - Gather and translate customer feedback into impactful product enhancements. - Partner with Engineering, Data Science, Sales, and Marketing to accelerate execution. - Oversee the full product lifecycle from ideation to scale. Hard Requirements - Proven track record building and scaling products in hyper-growth environments. - Founder/Early-stage startup experience (founding member or sub-20 person teams). - Demonstrated ability to design, launch, and scale products that deliver ### Senior Director of CMC and Nonclinical Program Management - Tonix Pharmaceuticals Holding Corp - Location: North Dartmouth, MA (unspecified) - Salary: $224K-$280K - Posted: 2026-03-19 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/tonixpharmaceuticals/jobs/4186570009 - Excerpt: Senior Director of CMC and Nonclinical Program Management North Dartmouth, MA Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix's CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit www.tonixpharma.com and follow the Company on LinkedIn and X . *Tonix's product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication. Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners. Position Overview Tonix ### Pharmaceutical Sales Specialist Immunology - Alsace - Regeneron Pharmaceuticals - Location: Remote - France (remote) - Salary: Not disclosed - Posted: 2026-06-08 - 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://regeneron.wd1.myworkdayjobs.com/Careers/job/Remote---France/Pharmaceutical-Sales-Specialist-Immunology---Alsace_R47580 - Excerpt: Pharmaceutical Sales Specialist Immunology - Alsace Remote - France posted: Posted 4 Days Ago ### Director, Commercial Operations and Analytics - Tonix Pharmaceuticals Holding Corp - Location: Berkeley Heights, NJ (unspecified) - Salary: $180K-$230K - Posted: 2025-12-15 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/tonixpharmaceuticals/jobs/4077936009 - Excerpt: Director, Commercial Operations and Analytics Berkeley Heights, NJ Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix's CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit www.tonixpharma.com and follow the Company on LinkedIn and X . *Tonix's product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication. Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners. Position Overview The Director, Commercial Operations ### Clinical Trial Assistant - Fortrea Holdings Inc - Location: Warsaw, Poland (unspecified) - Salary: Not disclosed - Posted: 2026-04-10 - 401(k) match: listed (not source-backed) - Apply: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Warsaw/Clinical-Trial-Assistant_261829/apply - Excerpt: Clinical Trial Assistant Warsaw, Poland Fortrea is looking for an experienced Clinical Trial Assistant to support global clinical studies within an FSP model for a leading pharmaceutical sponsor. What you'll do. Support clinical trials e... ### Pharmaceutical Technician II - Thermo Fisher Scientific - Location: Singapore, Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://thermofisher.wd5.myworkdayjobs.com/ThermoFisherCareers/job/Singapore-Singapore/Pharmaceutical-Technician-II_R-01340678/apply - Excerpt: Pharmaceutical Technician II Singapore, Singapore Embrace the role of a Pharmaceutical Technician II and play a vital role in sterile pharmaceutical production. Operate advanced equipment, ensure GMP compliance, and contribute to quality manufacturing. If you have hands-on experience in pharma production and a passion for safety and precision, this is your opportunity to make a difference. ### Vice President of Marketing - Nurix Therapeutics Inc - Location: Brisbane, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/nurix/jobs/8579556002 - Excerpt: Vice President of Marketing Brisbane, CA Company Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Position We are seeking a dynamic and experienced Vice President of Marketing with extensive experience launching new hematology / oncology products and incorporating commercial strategy into early development programs. The core objective is to build, lead and execute all aspects of Nurix Therapeutics marketing efforts. This individual will be responsible for developing all marketing strategies and tactical readiness for the commercialization of Nurix Therapeutics assets. In addition, this role will be accountable for driving commercial strategy in support of lifecycle management and our pipeline. Accountable for developing and executing all Global and US Marketing strategies that align with the overall company strategic imperatives. Ensure strategic alignment with cross-functional commercial partners in commercial insights and analytics, market access, and sales in order to produce high quality marketing efforts that achieve company performance objectives - Build and implement the marketing plan including, but not limited ### Scientist I (Contract), Drug Product Analytics - Vaxcyte Inc - Location: San Carlos, California, United States (unspecified) - Salary: $62-$68/hr - Posted: 2026-05-21 - 401(k) match: listed (not source-backed) - Apply: https://boards.greenhouse.io/vaxcyte/jobs/5224535008?gh_jid=5224535008 - Excerpt: Scientist I (Contract), Drug Product Analytics San Carlos, California, United States Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered. *AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary: Vaxcyte is looking for an energetic and talented individual to join our Drug Product Development team. The candidate must have knowledge of and practical experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) using a variety of methods, especially immunoassays and multiplexed immunoassay formats. Experience in analyzing vaccine and ### Sr CRA I - Fortrea Holdings Inc - Location: Buenos Aires, Buenos Aires, Argentina (unspecified) - Salary: Not disclosed - Posted: 2024-12-26 - 401(k) match: listed (not source-backed) - Apply: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Buenos-Aires/Sr-CRA-I_2434170/apply - Excerpt: Sr CRA I Buenos Aires, Buenos Aires, Argentina As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medi... ### Pharmaceutical Sciences, Technology & Innovation Lead (Sr. Director) - Takeda Pharmaceutical Company Limited - Location: Boston, MA (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Boston-MA/Pharmaceutical-Sciences--Technology---Innovation-Lead--Sr-Director-_R0178501-1 - Excerpt: Pharmaceutical Sciences, Technology & Innovation Lead (Sr. Director) Boston, MA posted: Posted Yesterday ### Senior Director, AIRx Biologics Discovery Lead - Takeda Pharmaceutical Company Limited - Location: Boston, MA (unspecified) - Salary: Not disclosed - Posted: 2026-06-09 - 401(k) match: listed (not source-backed) - Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Boston-MA/Senior-Director--AIRx-Biologics-Discovery-Lead_R0181772 - Excerpt: Senior Director, AIRx Biologics Discovery Lead Boston, MA posted: Posted 3 Days Ago ### Director, Commercial Regulatory Affairs, Labeling, Advertising, and Promotion - Syndax Pharmaceuticals Inc - Location: New York, NY (unspecified) - Salary: $225K-$250K - Posted: 2026-04-23 - 401(k) match: listed (not source-backed) - Apply: https://syndax.com/join-us/careers/?gh_jid=5978846004 - Excerpt: Director, Commercial Regulatory Affairs, Labeling, Advertising, and Promotion New York, NY Syndax Pharmaceuticals is looking for a Director, Commercial Regulatory Affairs, Labeling, Advertising, and Promotion At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies. The Role: We are currently seeking a qualified, highly motivated, experienced individual for the position of Director, Commercial Regulatory Affairs, Labeling, Advertising, and Promotion to lead labeling activities and the review of promotional materials in commercial regulatory affairs at Syndax for the company's 2 marketed FDA approved products in acute leukemia and chronic GVHD. The position reports to the Executive Director, Commercial Regulatory Affairs. The Director will lead and provide strategic input and oversight of regulatory labeling activities including labeling strategy for future indications of the lead company asset. The Director will lead the Labeling Working Group (LWG) meeting to develop an optimal Target Product Label (TPL), and U.S. Product Information (USPI) strategy and EU SmPC when applicable. This role will represent RA Labeling as the functional representative across the organizational levels relevant to assigned products and/or other activities. This role may include future responsibilities for managing, overseeing, reviewing, and approving the work of more junior staff related to labeling activities. This role will help to serve regulatory strategy in managing complex labeling negotiations with regulatory health authorities for future label expansion. This role also serves the as a ### Pharmaceutical Technician II - Thermo Fisher Scientific - Location: Singapore, Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://thermofisher.wd5.myworkdayjobs.com/ThermoFisherCareers/job/Singapore-Singapore/Pharmaceutical-Technician-II_R-01340680-1/apply - Excerpt: Pharmaceutical Technician II Singapore, Singapore Embrace the opportunity to become a Pharmaceutical Technician II and play a vital role in sterile pharmaceutical production. Operate advanced equipment, ensure GMP compliance, and contribute to quality manufacturing. If you have hands-on experience in pharma production and a passion for safety and precision, this is your opportunity to make a difference. ### Senior Director, Pharmaceutical Strategy and Development Leader - Crinetics Pharmaceuticals INC - Location: San Diego, CA (unspecified) - Salary: $214K-$268K - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/San-Diego-CA/Senior-Director--Pharmaceutical-Strategy-and-Development-Leader_JR000446 - Excerpt: Senior Director, Pharmaceutical Strategy and Development Leader San Diego, CA Crinetics is a pharmaceutical company based in San Diego, California that develops much-needed therapies for people with rare endocrine diseases. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and robust pipeline across preclinical and clinical development. We are driven by science with a patient-centric and team-oriented culture. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Come join our team as we transform the lives of others. Position Summary: The Senior Director, Pharmaceutical Development Team Leader (PDTL) is responsible for developing and leading the execution of comprehensive, compound-specific Technical Operations strategies to meet the global project team's (GPT) needs. This role provides leadership to interdisciplinary teams, managing multiple assets through various stages of development, and collaborates with various functional areas to achieve optimal development and business results. Essential Job Functions and Responsibilities: These may include but are not limited to: Develop, refine, update, and oversee Technical Operations project plans from multiple inputs, with emphasis on the alignment of these plans with strategic objectives, the decomposition of major objectives into discrete WBS-level work packages, the mapping of internal and cross-functional interdependencies, and the management of project risks. Perform detailed --- Source-backed benefit claims include source links; other benefit values are labeled separately.