Turn on analytics and we load Google Analytics: Google gets the pages you open and what you do here — searches, jobs you view, jobs you apply to — and sets its own cookies. Leave it off and the only cookies we set are your login, your theme, and this answer. Accept All also records a yes to advertising, which nothing uses yet. Privacy Policy.
3 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
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 ↗
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 ↗
Bristol Myers Squibb
Full-time · $275,630 – $374,075
This director-level role leads clinical strategy and medical due diligence for cardiovascular asset acquisitions at a pharmaceutical company, requiring a physician to evaluate trial designs, assess clinical risks, and guide deal feasibility across a therapeutic portfolio. It suits experienced cardiologists or internists with drug development background who want to shift into business development and shape which therapies the company pursues.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗