Senior PV Operations Lead for NDA Submissions

A clinical-stage biopharmaceutical company in the UK is seeking an experienced Senior Pharmacovigilance Operations Specialist. The role involves preparing safety data packages for regulatory submission, ensuring compliance with global regulations, and overseeing pharmacovigilance operations. Candidates should have 5+ years of experience in pharmacovigilance, proficiency in ICSR processing, and strong collaboration skills. This position offers an opportunity to contribute meaningfully to patient safety in therapeutic development.