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

Role: Lead pharmacovigilance activities for multiple products across various indications, ensuring patient safety throughout the product lifecycle. Responsibilities: oversee safety surveillance, signal detection, validation, assessment, and risk management strategies; develop and interpret safety data, author technical safety documents, and manage regulatory reporting such as PSURs and PADERs; lead and mentor Medical Directors and Associate Medical Directors; ensure compliance with pharmacovigilance regulations and guidelines. Requirements: MD/DO with 8-10 years of pharmacovigilance or clinical development experience; strong expertise in safety surveillance, regulatory guidance, and safety data analysis; effective cross-functional leadership and communication skills; proficiency in technical documentation and risk management. HighValue: pharmacovigilance, safety surveillance, signal detection, risk management, regulatory reporting, cross-functional leadership, global regulatory compliance, biologics or pharmaceutical products, product lifecycle management. WorkSetup: not specified; requires leadership and stakeholder engagement across clinical and regulatory teams.