Senior Pharmacovigilance Manager

Working remotely in a full-time capacity, the Senior Pharmacovigilance Manager will oversee safety assessment activities, manage reporting processes, and support clinical trial safety oversight within the Therapeutic Safety Teams. Key responsibilities Direct the planning, preparation, writing, and review of aggregate safety reports Organize and manage liaison activities with affiliates and internal partners regarding product safety Perform signal detection and evaluation, including data analysis and authoring safety assessment reports Required qualifications Doctorate degree with 2 years of industry pharmacovigilance experience, or a Master's degree with 4 years, or a Bachelor's degree with 6 years, or an Associate's degree with 10 years, or a high school diploma/GED with 12 years of experience Experience in clinical or medical research Preferred: Bachelor's in life science with a Master's and 6 years of related experience 2 years of managerial experience directly managing people or projects 6 years of experience in the biotech/pharmaceutical setting