Pharmacovigilance Specialist: SAE Data & Safety Reports

Worldwide Clinical Trials Limited is seeking an Associate, Pharmacovigilance to manage SAE data collection, evaluation, and reporting in compliance with regulatory guidelines and project instructions. The role involves creating safety plans, reviewing data for completeness, and maintaining data integrity across systems. You will generate queries, perform QA of SAEs, and contribute to regulatory submissions while interacting with global clients and sites. #J-18808-Ljbffr Worldwide Clinical Trials Limited