Pharmacovigilance Scientist

A company is looking for a Pharmacovigilance Scientist.

Key Responsibilities :

Collects, reviews, and analyzes adverse event reports from clinical trials to identify potential safety signals

Assesses clinical safety data to identify and document adverse events and emerging safety concerns

Supports the preparation and review of pharmacovigilance documents and ensures compliance with safety regulations

Qualifications :

Advanced degree in life sciences (e.g., PharmD, PhD) or related field

Minimum of 3 years of experience within the pharmaceutical industry, ideally including drug safety experience

Knowledge of good pharmacovigilance practices and drug safety regulations

Understanding of pharmacovigilance regulatory practices including CIOMS, EMA, ICH, and FDA guidelines

Experience with adverse event data review and safety database management (e.g., Argus, MedDRA, Veeva Vault)