FSP CRA II（Wuhan）
Fortrea(3 days ago)
About this role
A Clinical Research Associate (CRA) at Fortrea oversees the monitoring and management of clinical studies, ensuring compliance with regulatory guidelines and data integrity. The role involves site management, regulatory documentation, and collaboration with study teams to facilitate successful clinical trials.
Required Skills
- GCP
- ICH Guidelines
- Monitoring
- Regulatory
- Clinical Trials
- Data Management
- eCRF
- Site Management
- SAE Reporting
- Medical Devices
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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