Are you an experienced Senior Pharmacovigilance Scientist? Are you interested in overseeing and leading the process for safety signal management activities and aggregate reports? If so, we would love to speak with you. We are hiring for a Senior PV Scientist to join a globally leading Biotechnology client of ours, ensuring products in clinical trials continue to maintain good standing with countries where studies are ongoing to ensure clinical studies are completed, and for marketed products, ensuring the marketing authorisation remains in good standing. The successful candidate will be responsible for acting as product lead for Pharmacovigilance activities within Safety. You will also be responsible for overseeing and leading the process for safety signal management activities, aggregate reports, responding to safety questions from internal and external stakeholders, reviewing medical and scientific literature for safety information, and supporting Clinical Trial PV medical activities. This is a contract position, offered initially for 12 months working 37.5 hours per week based in Maidenhead. (Inside IR35). Responsibilities: Leads the signal management process (i.e., signal detection, signal tracking, signal documentation, facilitating decisions regarding signals and safety risk, etc.) for assigned product(s) and evaluates safety data and signals as part of ongoing pharmacovigilance activities. Synthesis of data from multiple s...