FSO CRA (Guangzhou)
Fortrea(14 days ago)
About this role
This role involves site management and monitoring responsibilities for clinical studies, ensuring compliance with regulatory guidelines and quality standards. The position offers an opportunity to work in a collaborative environment supporting the successful execution of clinical trials across various phases.
Required Skills
- ICH GCP
- Clinical Monitoring
- Source Data Verification
- Regulatory Compliance
- Clinical Trials
- eClinical Systems
- SAE Reporting
- Site Management
- Data Integrity
- Protocol Adherence
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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