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25 open listings
Roles posted by organizations here, alongside roles we found on employers’ own careers sites. Crawled roles say so on the card and send you to the employer to apply. Only show organizations on Career App
Beckman Coulter
Full-time · 2 locations · $120,000 – $165,000
This role leads clinical trial strategy and design for diagnostic products across US and EU markets, supporting regulatory submissions and product commercialization. It suits experienced clinical scientists with deep knowledge of diagnostic device development and regulatory pathways who want to influence global healthcare through strategic study leadership.
Listed on Beckman Coulter’s careers site · Apply there ↗
Biogen
Full-time · Cambridge, MA · $188,000 – $259,000
This director-level role leads a team building data systems and intelligence to monitor risks across Biogen's manufacturing and supply network, translating complex operational data into executive guidance for strategic decisions. The position suits experienced analytics leaders with deep pharmaceutical manufacturing knowledge who can combine technical rigor with clear stakeholder communication.
Merck
Full-time · $173,200 – $272,600
This role leads global regulatory strategy for vaccine and infectious disease products, serving as the primary regulatory contact between the company, FDA, and international agencies throughout drug development and commercialization. It suits experienced scientists with strong command of pharmaceutical regulation and the ability to work independently on complex, multi-indication programs.
Listed on Merck’s careers site · Apply there ↗
Bristol Myers Squibb
Full-time · $226,750 – $313,460
A senior regulatory leadership role at a major pharmaceutical company guiding the development and commercialization of neuroscience drugs globally. This position suits experienced regulatory professionals with scientific backgrounds who can navigate complex drug development, interface with health authorities, and lead strategic initiatives across multiple markets.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Moderna
$210,900 – $379,200
Lead global medical strategy and scientific direction for Moderna's oncology mRNA programs from early development through commercialization, managing cross-functional teams and external stakeholder relationships. Ideal for an experienced medical affairs leader with deep oncology expertise who thrives in fast-paced, matrix environments and wants to shape the future of cancer treatment.
Listed on Moderna’s careers site · Apply there ↗
Gilead Sciences
Full-time · United States - California - Foster City · $226,185 – $292,710
This role leads ethics and compliance efforts for Gilead's HIV prevention and treatment business, serving as a trusted advisor to commercial, medical, and legal teams on regulatory and compliance matters. The position requires extensive experience in pharmaceutical or biotech compliance, with proven ability to manage a team and navigate complex healthcare regulations.
Listed on Gilead Sciences’s careers site · Apply there ↗
Hims and Hers
Full-time · New Albany, OH
This role oversees regulatory compliance and quality assurance for a high-volume non-sterile compounding pharmacy, serving as the Designated Person to ensure operations meet federal and state standards. It suits an experienced pharmacist with compounding expertise who thrives in regulated environments and can translate complex requirements into practical workflows.
Listed on Hims and Hers’s careers site · Apply there ↗
Astranis
San Francisco, CA · $140,000 – $200,000
A satellite network design engineer at a space communications company, balancing technical analysis with customer-facing sales engineering to optimize high-throughput satellite networks for commercial and government clients. This role suits experienced satellite systems professionals comfortable with complex trade-off analysis and vendor management.
Listed on Astranis’s careers site · Apply there ↗
Biogen
Full-time · Cambridge, MA · $278,000 – $382,000
Lead medical affairs strategy and execution across Biogen's neuropsychiatry portfolio, managing cross-functional teams and serving as the senior medical authority for this therapeutic area. This role suits experienced medical leaders from clinical or scientific backgrounds who are ready to drive strategic impact in a complex, multi-product environment.
Listed on Biogen’s careers site · Apply there ↗
Merck
Full-time · $282,200 – $444,200
This role leads clinical research strategy and execution for blood cancer medicines across all development phases, from early-stage work through post-market studies. It suits experienced physician-scientists who want to shape drug development strategy and collaborate across functional teams in a large pharmaceutical environment.
Listed on Merck’s careers site · Apply there ↗
Bristol Myers Squibb
Full-time · $255,860 – $347,244
A Director-level physician role overseeing medical safety strategy and risk management for Bristol Myers Squibb's neuroscience compounds throughout development and post-market phases. This position suits experienced medical doctors with pharmacovigilance or clinical research backgrounds who can lead cross-functional safety teams and interact with regulators.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Gilead Sciences
$237,575 – $338,250
This role leads a biostatistics team across one or more therapeutic areas, setting statistical strategy and advising senior leadership on development priorities. It suits experienced biostatisticians ready to build teams, shape company-wide data practices, and influence drug development decisions at an executive level.
Listed on Gilead Sciences’s careers site · Apply there ↗
Merck
Full-time · Rahway, NJ · $156,900 – $247,000
A senior scientific leadership role directing the analytical characterization of biologic drugs, suitable for an experienced analytical chemist or biochemist ready to lead a team while developing advanced testing methods for complex protein-based medicines.
Listed on Merck’s careers site · Apply there ↗
Bristol Myers Squibb
Full-time · $150,300 – $182,125
This role leads safety surveillance and risk management for pharmaceutical products throughout their lifecycle, working with medical safety teams to detect signals, prepare regulatory documents, and ensure compliance. It suits experienced pharmacovigilance professionals who can independently manage complex safety strategies and mentor others in a matrix environment.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Gilead Sciences
Full-time · United States - California - Foster City · $349,010 – $451,660
This role leads clinical development strategy and execution for inflammation and immunology programs at Gilead, managing complex multi-indication portfolios from early phase through Phase 3 trials. It suits experienced physician-scientists with strong regulatory and drug development backgrounds who can lead cross-functional teams and represent programs to health authorities.
Listed on Gilead Sciences’s careers site · Apply there ↗
Merck
Full-time
Lead the oncology medical affairs function across Estonia, Latvia, and Lithuania for a major pharmaceutical company, managing a small team and developing regional strategy while engaging with scientific stakeholders and supporting global initiatives. Suited to an experienced medical professional with oncology background and demonstrated ability to manage people and navigate matrix organizations.
Listed on Merck’s careers site · Apply there ↗
Bristol Myers Squibb
Full-time · 2 locations · $275,630 – $374,075
A senior physician role overseeing multiple clinical trials in neuroscience drug development at a large pharmaceutical company, responsible for medical safety, regulatory strategy, and scientific leadership across global trial programs.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Gilead Sciences
Full-time · $153,935 – $219,120
This role leads medical information strategy and scientific communications for Gilead's pharmaceutical products, responding to healthcare provider and patient inquiries while managing complex regulatory compliance and cross-functional initiatives. It suits experienced medical affairs professionals or scientists with deep pharmaceutical knowledge who can synthesize clinical data and lead teams in a matrixed environment.
Listed on Gilead Sciences’s careers site · Apply there ↗
Bristol Myers Squibb
Full-time · $215,130 – $291,964
A leadership role overseeing global and US regulatory strategy for drug development programs, working across internal teams and external partners to navigate approvals and bring products to market. This suits experienced regulatory professionals ready to own complex, multi-market registration strategies and lead cross-functional teams at scale.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Gilead Sciences
United States - California - Foster City
This is a senior clinical leadership role overseeing the development of anti-inflammatory and autoimmune disease treatments across multiple programs and therapeutic areas. The position suits experienced physician-scientists or Ph.D. holders with substantial pharmaceutical industry background who can manage complex drug portfolios, external partnerships, and cross-functional teams.
Listed on Gilead Sciences’s careers site · Apply there ↗
Bristol Myers Squibb
Full-time · $164,110 – $228,701
A pharmaceutical biostatistician role supporting clinical trial design and regulatory submissions at a major drug manufacturer. This position suits someone with a strong statistical foundation and 3–5+ years' experience in pharmaceutical development who wants to grow into team leadership.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Gilead Sciences
Full-time · United States - California - Foster City · $210,375 – $272,250
This role leads ethics and compliance support within Gilead's U.S. market access function, advising cross-functional teams on regulatory and compliance matters in the pharmaceutical industry. It suits experienced healthcare compliance professionals with management capability who can serve as trusted advisors to commercial and medical teams.
Listed on Gilead Sciences’s careers site · Apply there ↗
Bristol Myers Squibb
Full-time · Princeton, NJ · $239,080 – $289,708
This executive-level role leads commercial strategy for Bristol Myers Squibb's neuroscience portfolio, focusing on the KarXT asset and emerging areas like schizophrenia and Alzheimer's disease psychosis. It suits experienced pharma leaders comfortable translating clinical potential into global market strategy and influencing across complex organizations.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Gilead Sciences
Full-time · United States - California - Foster City · $261,375 – $338,250
This role leads clinical development programs for inflammation and fibrosis therapies at a major biopharmaceutical company, overseeing trial design, regulatory submissions, and cross-functional coordination. It suits physicians with significant drug development experience who want to shape late-stage therapeutic programs while providing medical oversight.
Listed on Gilead Sciences’s careers site · Apply there ↗
Gilead Sciences
Full-time · 2 locations · $195,670 – $253,220
Lead biostatistical strategy and analysis for clinical development programs in an inflammatory disease therapeutic area, managing statistical teams and representing the function across multiple studies and regulatory interactions. This role suits experienced biostatisticians ready to step into leadership of both technical statistical work and people management at a large pharmaceutical company.
Listed on Gilead Sciences’s careers site · Apply there ↗
Listed on Biogen’s careers site · Apply there ↗