Safety Aggreg Report Spec 2

This role serves as a signal detection and literature lead for ongoing safety surveillance of marketed and investigational products within a pharmacovigilance team. The incumbent is responsible for authoring aggregate reports, managing regulatory inquiries, and overseeing end-to-end signal management deliverables for specific molecules. Key duties include collaborating with cross-functional stakeholders, ensuring compliance with SOPs, and maintaining in-depth knowledge of assigned disease areas and molecules.