Sr Pharmacovigilance Scientist

Role: Senior Pharmacovigilance (PV) Scientist leading safety signal management and aggregate reporting for biopharma products. Responsibilities include managing signal detection, authoring PSURs/DSURs, handling safety inquiries, and supporting clinical trial PV activities. The role involves collaboration with global safety teams, regulatory agencies, and cross-functional partners, ensuring compliance with international safety regulations. Qualifications: Bachelor’s in biological sciences or healthcare; advanced degree (PhD, MPH, PharmD, NP) preferred; significant PV experience with expertise in safety signals, aggregate reports, and regulatory interactions. Skills: strong data interpretation, scientific communication, project leadership, and proficiency with safety databases and standard data tools. Experience in biologics or small molecules, with a focus on clinical development and post-market safety surveillance, is highly valued. The position is management-level, emphasizing leadership, mentorship, and cross-team coordination. The role supports products across clinical trial phases and marketed portfolios, with a focus on global regulatory compliance. Location details and travel are not specified.