Associate Director, Safety Data Sciences

Role: Pharmacovigilance Scientist specializing in product safety surveillance throughout the product lifecycle. Responsibilities: monitor safety data from clinical trials, literature, and databases; analyze signals and prepare regulatory and safety assessments; communicate safety findings to internal teams and senior management; author and review safety reports, Clinical Study Reports, and Risk Management Plans; support risk minimization activities and regulatory compliance. Requirements: degree in Health Sciences (Pharmacy, Epidemiology, Nursing); 4+ years (bachelor’s) or 2+ years (master’s/PhD) experience in clinical or safety roles; deep knowledge of drug development, pharmacovigilance regulations, and safety data analysis tools; strong communication and project management skills; proficiency in Microsoft Word and Excel. High-Value: focus on safety monitoring for biologics or small molecule products, with involvement in global regulatory activities; collaborative role with cross-functional teams across clinical, regulatory, and safety domains. Work setup: location flexible across AbbVie hubs; no travel specified.