Senior Pharmacovigilance Manager

Job Summary

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