Pharmacovigilance Specialist
3 days ago
At Medpace, we are seeking a highly motivated Pharmacovigilance Specialist to join our Clinical Safety team in Stirling. As part of a high-performing group, this position plays a key role in accomplishing tasks and working on projects that contribute to the development of life-changing medicines. The successful candidate will be responsible for collecting, processing, and tracking serious adverse event reports, generating safety narratives and queries, and performing quality control of safety cases.
We offer a competitive salary of approximately £40,000 per annum, commensurate with experience.
Responsibilities- SAE Reporting: Collect, process, and track serious adverse event reports
- Safety Narratives and Queries: Generate safety narratives and queries
- Safety Database Management: Perform quality control of safety cases and manage safety databases
- Minimum Bachelor's degree in a life science field
- 2+ years of experience in Clinical Trial Pharmacovigilance
- Working knowledge of Safety Databases (Argus is desirable)
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