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Senior Pharmacovigilance Lead — Safety Data & Submissions

Worldwide Clinical Trials, Durham, NC, United States


A leading global clinical research organization is looking for a Senior Drug Safety, Pharmacovigilance professional in North Carolina. The role involves overseeing the collection and reporting of Serious Adverse Event data, authoring Safety Management Plans, and mentoring team members. Candidates should have a Bachelor's degree in a science-related field, with at least 5 years of experience in pharmacovigilance. Strong knowledge of medical terminology and regulatory requirements is essential. This position offers an opportunity to contribute towards improving lives through clinical research. #J-18808-Ljbffr