- Beijing, China
- 2+ years
Clinical Research Associate responsible for site monitoring, data integrity, and regulatory compliance for clinical trials in Beijing.
Responsibilities
- Conduct site monitoring visits including pre-study, initiation, routine, and close-out
- Verify study training records and informed consent procedures
- Review source documents and generate queries
- Maintain eTMF and sponsor documents
- Track investigational product inventory
Requirements
- University or college degree, or certification in a related allied health profession
- Nice to have: Phase I monitoring experience
- Nice to have: Life Science or Nursing qualification
- Nice to have: Fortrea SOPs knowledge
- Nice to have: additional years in related field