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4 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
Merck
Full-time
This role leads clinical safety and pharmacovigilance strategy for approved medications, chairing cross-functional teams and overseeing risk management plans, safety surveillance, and regulatory documentation. It suits experienced physicians with at least 7 years in industry and 4+ years managing drug safety, who can synthesize complex safety data and guide organizational strategy.
Listed on Merck’s careers site · Apply there ↗
IQVIA
This role oversees medical safety and pharmacovigilance for a CRO's client programs, reviewing trial data and regulatory documents while leading a team of physicians and safety professionals. It suits experienced medical safety physicians who want to manage complex, multi-stakeholder projects with both clinical and people leadership responsibilities.
Listed on IQVIA’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 ↗
Merck
Full-time
A medical specialist responsible for reviewing adverse event reports and developing safety strategies for pharmaceutical products in collaboration with physicians and cross-functional teams. This role suits someone with clinical background and drug safety expertise who can manage complex regulatory and pharmacovigilance responsibilities.
Listed on Merck’s careers site · Apply there ↗