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

Role: Lead pharmacovigilance activities as a Medical Director overseeing product safety for AbbVie's pharmaceutical/biological products throughout their lifecycle. Responsibilities: manage safety surveillance, develop and execute safety strategies, lead safety documentation including medical safety assessments and risk management plans, and oversee aggregate safety data analysis and communication. Provide technical input on regulatory safety reports (e.g., PSURs, PADERs), oversee safety activities across multiple indications and products, and implement risk mitigation strategies. Lead and mentor safety teams, managing performance and talent development. Qualifications: MD/DO with 8-10 years of pharmacovigilance and clinical development experience, including expertise in safety surveillance for pharma/biotech products. Additional: deep understanding of pharmacology, toxicology, and regulatory guidance; strong analytical, communication, and leadership skills; experience in managing cross-functional teams; fluency in English. High-Value: roles focus on product safety in immunology, oncology, or neuroscience, with responsibilities spanning clinical trial safety and post-marketing surveillance. Work setup: location details not specified, likely hybrid or onsite given seniority and oversight scope.