Scientific Director, Oncology - Global Patient Safety

Role: Senior Safety Scientist supporting oncology assets throughout their lifecycle, focusing on risk assessment and benefit-risk analysis. Responsibilities: contribute to safety strategy development, review and synthesize safety data for regulatory and clinical documents (IBs, DSURs, PSURs, RMPs, CSRs), facilitate cross-functional scientific interactions, and assist in due diligence activities related to oncology assets. Also, support process improvements within the safety team. Requirements: scientific or clinical degree (NP/PA, PharmD, MS, PhD, MPH), 5+ years in pharmacovigilance or clinical development within the pharmaceutical industry, strong analytical skills in oncology safety data, knowledge of clinical trial methodology, regulatory compliance, and safety document preparation. Preferred: experience in biological sciences, oncology-specific safety assessment, and cross-functional influence. HighValue: oncology, clinical safety, risk management, regulatory documentation, pharmacovigilance, lifecycle safety strategy. WorkSetup: unspecified; emphasis on cross-functional collaboration and scientific rigor.