Director, Pharmacovigilance

Provide scientific and operational pharmacovigilance support for Beam’s therapeutic portfolio. Responsibilities span review of individual and cumulative safety data, signal assessment, risk management, aggregate safety reports and collaboration with clinical development teams. The director also oversees safety vendors and contributes to clinical and regulatory documents. The Cambridge role requires one to three days per week onsite.

Relevant pharmacy, nursing, epidemiology or bioscience qualification; a healthcare professional degree is preferred. Typically at least 12 years in the pharmaceutical industry, including five in pharmacovigilance. Requires safety-data interpretation, global safety regulations and safety-database experience.