FSP CRA II(Wuhan)
Fortrea(26 days ago)
About this role
A Clinical Monitoring role for individuals overseeing the conduct of clinical studies, ensuring compliance with regulatory, ethical, and quality standards. The position involves site management, data verification, and collaboration with study teams to ensure trial integrity and subject safety.
Required Skills
- ICH GCP
- Clinical Monitoring
- Regulatory Compliance
- Source Data Verification
- Trial Management
- eClinical Systems
- Data Integrity
- SOPs
- Site Management
- SAE Reporting
About Fortrea
fortrea.comFortrea, a leading CRO, advancing clinical trials through patient-focused clinical solutions that accelerate clinical development, drive trial success, and bring innovative therapies to those who need them most.
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