Worldwide Clinical Trials is seeking an Associate in Pharmacovigilance to oversee SAE data collection, evaluation, and reporting for studies of varying complexity.
You will lead safety activities with support from senior staff and ensure data integrity and regulatory compliance.The role requires a science background, at least 1 year in pharmacovigilance, strong communication, and proficiency with MS Office.
Domestic/international travel may be needed as projects demand.
#J-*****-Ljbffr