Offer summary
Qualifications:
Strong knowledge of GCP regulations, 6 years' clinical trial management experience, Experience with study start-up and closeout, DEC/IRB applications.
Key responsabilities:
- Lead and manage CTIMP and non-CTIMP trial programs
- Coordinate project partners and oversee project progress
- Facilitate team training; collaborate with tech and product teams
- Contribute to clinical strategy and business development
- Support inspection readiness and develop risk mitigation strategies