Director, Medical Safety Assessment Physician

Role: Lead medical safety assessment for Bristol Myers Squibb, focusing on pharmacovigilance activities across multiple compounds and development stages. Responsibilities: oversee safety signal evaluation, prepare aggregate safety reports (e.g., DSUR, PBRER), lead benefit-risk strategies, contribute to safety labeling and regulatory submissions, support postmarketing safety activities, and drive PV process improvements. Collaborate with global health authorities, DMCs, and cross-functional teams including clinical, regulatory, and medical affairs. Requirements: MD or equivalent with 3+ years in PV or relevant biomedical/pharmaceutical fields; strong knowledge of drug development, safety assessment, regulatory requirements, and observational research tools. Preferred: postgraduate qualification in internal medicine, immunology, oncology, or related specialty. HighValue: expertise in biologics or small molecules, experience in clinical development, postmarketing safety, and global regulatory interactions, with occasional US and international travel. WorkSetup: flexible, with potential for onsite, hybrid, or remote work.