Pharmacovigilance Specialist
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Accentuate Staffing is seeking a Pharmacovigilance (PV) Specialist to support a cutting edge biotechnology organization in RTP. The Pharmacovigilance (PV) Associate will be responsible for performing retrospective quality review of the data collected from the CRO
This is a long term contract position lasting up to one year. Candidate should be able to work on site in RTP 3 times per week, remote 2 times per week.
Responsibilities:
- Responsible for performing retrospective quality review of clinical trial data from the CRO
- Work collaboratively with internal and external teams
- Perform data entry, quality control checks, and review of all documentation using Argus database
Requirements:
- Experience performing data entry/processing working at a biotech and/or pharmaceutical organization in a Pharmacovigilance capacity
- Retrospective Quality Reviewing experience
- Hands-on experience using Argus is required
- Bachelor of Science in health/science related field
