FSP CRA II（Changsha）
Fortrea(21 days ago)
About this role
A Clinical Research Associate (CRA) at Fortrea is responsible for site management and monitoring of clinical studies, ensuring compliance with regulatory guidelines and safeguarding data integrity. The role involves coordinating site activities, verifying subject safety, and maintaining study documentation to support successful trial execution.
Required Skills
- ICH GCP
- Clinical Monitoring
- Regulatory Compliance
- Source Data Verification
- Clinical Trial Management
- Medical Devices
- Data Integrity
- eClinical Systems
- 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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