Worldwide Clinical Trials is seeking a pharmacovigilance professional with 5+ years of pre‑approval PV experience to support safety data management and regulatory submissions. You will review SAE data, maintain safety databases, and generate safety reports while coordinating with global teams.
The role requires strong MS Office skills, excellent communication, and the ability to work independently within a matrix environment.
#J-18808-LjbffrSenior Pharmacovigilance Associate - Japan (Remote) in workfromhome at Unknown Company
This position is listed as full time and onsite.