Associate Director, Safety Data Sciences

Role: Pharmacovigilance Scientist responsible for safety monitoring of assigned products throughout their lifecycle, including signal detection, evaluation, and risk communication. Responsibilities: analyze safety data from clinical trials, literature, and databases; develop strategies for signal assessment; prepare safety summaries, regulatory reports, and risk management documents; communicate safety findings to internal teams and regulatory authorities; mentor junior staff. Requirements: degree in a Health Sciences field (Pharmacy, Epidemiology, Nursing); 4+ years (Bachelors) or 2+ years (Masters/PhD) in clinical/pharma or safety; strong knowledge of drug development, regulatory safety standards, and pharmacovigilance guidelines; proficiency in safety data analysis tools, Microsoft Office, and project management; effective communication skills. HighValue: experience with biologics or small molecules in immunology, oncology, or neuroscience; familiarity with global safety reporting and regulatory submissions; ability to work independently in a cross-functional, matrix environment. WorkSetup: multiple hub locations in the US; specific travel requirements not stated.