Senior Safety Data Scientist

Role: Pharmacovigilance Scientist supporting product safety and benefit-risk assessments across AbbVie's portfolio, focusing on signal detection, evaluation, and safety communication throughout the product lifecycle. Responsibilities: review safety data from clinical trials, literature, and databases; collaborate with clinical and safety teams to develop assessment strategies; analyze data for signal evaluation and regulatory safety requests; communicate safety findings to internal stakeholders and regulatory bodies; contribute to safety documentation such as CSRs, risk management plans, and safety summaries; ensure compliance with pharmacovigilance regulations and company SOPs. Requirements: degree in Health Sciences (e.g., Pharmacy, Epidemiology, Nursing); 2+ years' clinical/pharma or safety experience for Bachelors, or 1-2 years for Masters/PhD; knowledge of drug development, clinical trials, and regulatory safety standards; proficiency in safety data analysis and communication skills. HighValue: pharmacovigilance, signal detection and evaluation, safety reporting, regulatory interactions, clinical safety data management. WorkSetup: not specified.