Scientific Director, Immunology, Global Patient Safety

Role: Senior safety scientist supporting immunology assets throughout their lifecycle, leading safety strategy development and implementation. Responsibilities: review and synthesize scientific safety data for regulatory and clinical documents (e.g., IBs, DSURs, RMPs, CSRs); facilitate cross-functional scientific interactions; prepare competitive intelligence and disease state analyses; draft presentations for internal/external meetings; collaborate with Clinical Development, Regulatory, Medical Affairs, and other teams to ensure comprehensive safety assessments; drive process improvements within the safety team; conduct literature reviews and propose safety actions. Requirements: scientific or clinical degree (NP/PA, PharmD, MS, PhD, MPH); 5+ years in pharma, preferably in patient safety/Pharmacovigilance; knowledge of clinical trial methodology, regulatory compliance, clinical strategy development; strong data analysis and interpretation skills; effective communicator and influencer; ability to operate under uncertainty and complexity. HighValue: immunology therapeutic area, safety/pharmacovigilance focus, regulatory document development, cross-functional collaboration, literature review skills. WorkSetup: not specified, but likely office-based or hybrid, given cross-team interactions.