Head of Multiple Myeloma & AML, Oncology - Global Patient Safety
AbbVie
September 02, 2026
Full-time
Remote friendly (Irvine, CA)
Worldwide
$504,500 - $504,500 USD yearly
Clinical Research and Development
Role: Lead pharmacovigilance and patient safety activities for AbbVie's products, overseeing safety surveillance from clinical development through post-market. Responsibilities: manage safety teams, develop and execute strategies for safety assessments, signal detection, and risk management; author and review pharmacovigilance documents including PSURs and risk plans; interpret aggregate safety data and communicate findings cross-functionally; ensure compliance with regulatory requirements; oversee safety activities across multiple indications or related products; mentor and evaluate team members. Qualifications: MD/DO with 8-10 years in pharmacovigilance or clinical development; 2+ years residency with patient management; experience analyzing clinical and epidemiological data; strong technical writing skills; ability to lead cross-functional teams; effective communication in English; preferred: Master of Public Health. High-Value: pharmacovigilance, product safety, clinical trial and post-marketing oversight, signal detection, risk management, regulatory compliance, global safety standards, cross-product safety strategy, team leadership. WorkSetup: Not specified.