Job Description
About This Role
As the Associate Director for the Safety Surveillance and Aggregate Reports group, you will play a pivotal role in ensuring the safety and efficacy of our products while fostering a collaborative and high‑performing team environment. Your responsibilities include leading pharmacovigilance activities for specific products, providing strategic direction and scientific oversight, overseeing signal detection, managing the creation and review of aggregate reports, and leading the development of Risk Management Plans (RMPs). The role also involves responding to regulatory requests and ensuring comprehensive safety surveillance. This position is critical to maintaining patient safety and compliance with global PV regulations, driving operational efficiencies, fostering cross‑functional collaboration, and contributing to organizational projects and goals. It is a hybrid role, requiring 50% of each week on site at our Maidenhead office.