Offer summary
Qualifications:
College degree or 2+ years of education in a related field, At least 10 years of related experience in clinical and regulatory document review or medical editing, Experience with Veeva, SharePoint, PerfectIt, and StartingPoint is a plus.
Key responsabilities:
- Ensure accuracy of clinical and regulatory documents
- Train and supervise clinical editors
- Perform quality reviews and detailed data accuracy checks
- Substantively edit and proofread documents
- Contribute to periodic quality control process reviews