Head of Multiple Myeloma & AML, Oncology - Global Patient Safety

Role: Lead pharmacovigilance activities as a Medical Director, overseeing product safety strategies across multiple indications and product lifecycles. Responsibilities: manage safety surveillance for pharmaceutical, biologic, and combination products; develop and oversee PV documents including safety assessments, risk management plans, and periodic reports (e.g., PSURs, PADERs); interpret aggregate safety data and ensure regulatory compliance; lead cross-functional teams, mentor staff, and coordinate safety activities at the product level. Qualifications: MD/DO with 8-10 years in pharmacovigilance or clinical development, including experience in safety data analysis, regulatory submissions, and risk management; strong leadership, communication, and collaboration skills; fluency in English; residency training plus additional public health qualifications preferred. HighValue: pharmacovigilance, product safety, signal detection, risk management, regulatory compliance, cross-industry pharmacovigilance experience, safety document authorship, therapeutic areas including immunology, oncology, neuroscience. WorkSetup: role details on location/modality and travel are not specified.