FSO CRA II (Beijing)
Fortrea(28 days ago)
About this role
A Clinical Research Associate (CRA) at Fortrea is responsible for managing and monitoring clinical studies to ensure compliance with regulatory standards, protocol adherence, and data integrity. The role involves site visits, training, and collaboration with study teams to support the successful execution of clinical trials.
Required Skills
- ICH GCP
- Clinical Monitoring
- Source Data Verification
- Regulatory Compliance
- eCRF
- Clinical Trials
- SAE Reporting
- Trial Management
- Investigator Management
- Data Review
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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