Senior Pharmacovigilance Manager

Working remotely in a full-time capacity, the Senior Pharmacovigilance Manager will oversee safety assessment activities, manage the preparation and review of aggregate reports, and support clinical trial safety oversight in the obesity therapeutic area. Key responsibilities Direct the planning, writing, and review of aggregate safety reports and manage communications with affiliates Review adverse events from clinical trials and participate in safety data analysis and signal detection Assist in the development of risk management strategies and support regulatory filings related to safety activities Required qualifications Doctorate degree with 2 years, Master's degree with 4 years, Bachelor's degree with 6 years, Associate's degree with 10 years, or High school diploma/GED with 12 years of industry pharmacovigilance experience Preferred Bachelor's in life science and Master's with 6 years of related experience 2 years of managerial experience directly managing people or projects Clinical or medical research experience 6 years of experience in the biotech/pharmaceutical setting