Director, Medical Safety Assessment Physician

Role: Lead safety activities and benefit-risk assessments for Bristol Myers Squibb's compounds, chairing product Safety Management Teams and serving as the safety subject matter expert. Responsibilities: oversee safety review documents, evaluate and manage safety signals, lead safety labeling activities, support regulatory interactions, and drive process improvements within pharmacovigilance (PV). Provide safety input for clinical development, postmarketing safety, and regulatory submissions; collaborate with cross-functional teams including regulatory, medical, and manufacturing; support health authority meetings and safety communications. Qualifications: MD or equivalent, with 3+ years in PV or relevant biomedical fields; postgraduate training in internal medicine, immunology, oncology, or related areas preferred. Skills include understanding of drug development, PV regulations, safety signal analysis, and risk management; excellent communication, analytical, and multitasking abilities. High-Value: focus on biologics or small molecules in clinical or post-approval stages; experience with safety reporting, benefit-risk strategies, and global safety operations; occasional travel within US and abroad. Work setup: role specifics on location are not specified, but flexible work environment implied.