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Pharmacovigilance

Healthcare and Medical

Pharmacovigilance is the science of detecting, assessing, and preventing adverse drug reactions and other drug-related problems, often after a medication reaches the market. It is practiced by regulatory agencies, pharmaceutical companies, and safety scientists to monitor drug safety throughout a product's lifecycle.

Pharmacovigilance in the job market

Last checked October 28, 2026

Open roles
4

on Career App

Employers
3

hiring for it

Median pay
—

not enough disclosed

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Open roles requiring Pharmacovigilance (4)

Merck

Clinical Safety and Risk Management Principal Scientist

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

Director, Medical Safety- Sponsor-Dedicated (Home-based)

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

Senior Director, Medical Safety Assessment Program Lead, Neuroscience

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

Clinical Safety and Risk Management Associate Principal Scientist

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 ↗

Roles that use Pharmacovigilance

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