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

Role: Senior Medical Director leading product safety teams within pharmacovigilance, overseeing safety assessments across multiple products and lifecycle stages. Responsibilities: develop and implement strategies for safety surveillance, signal detection, and risk management; author and review safety documentation including PSURs, PADERs, and risk plans; interpret clinical, pharmacological, and non-clinical data; ensure compliance with regulatory guidelines; mentor and manage medical safety teams; coordinate safety activities across indications and products. Requirements: MD/DO with 8-10 years in pharmacovigilance or clinical development; strong expertise in safety surveillance, data analysis, and regulatory standards; leadership experience in cross-functional teams. High-value: pharmacovigilance, product safety, signal detection, risk management, regulatory compliance, post-marketing surveillance, cross-functional leadership. Work setup: not specified.