- Remote, China
- Remote
- 1+ years
Clinical Research Associate (CRA) responsible for monitoring and managing clinical trial sites, ensuring compliance with protocols, ICH-GCP guidelines, and regulatory requirements.
Compensation
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits.
Responsibilities
- Monitor investigator sites using risk-based monitoring.
- Conduct on-site and remote visits to assess protocol compliance.
- Review and verify data accuracy through SDR, SDV, and CRF.
- Document observations and communicate findings.
- Escalate deficiencies and follow up to resolution.
Requirements
- Bachelor's degree in a life sciences related field or Registered Nursing certification