Senior Medical Director, Pharmacovigilance

Role: Senior Medical Director, Pharmacovigilance, overseeing global safety monitoring for marketed and investigational biopharma products, with a focus on kinase inhibitors for cancer. Responsibilities: lead benefit-risk assessments, manage safety surveillance activities, review adverse event reports, contribute to regulatory safety documents, and support risk management plans. Serve as a medical expert in cross-functional teams, lead safety data reviews, and guide decision-making on safety issues. Requirements: MD (board certification preferred), 10+ years in pharmacovigilance or drug safety within biotech/pharma, strong scientific/clinical background, proficiency in safety data assessment, and knowledge of global pharmacovigilance regulations. Preferred: broad therapeutic expertise, experience with digital safety tools, process optimization, and cross-cultural team leadership. High-value: extensive experience in oncology, kinase inhibitors, global regulatory environment, and safety data analysis. Work setup: not specified; likely fully remote or hybrid given global scope.