FSP CRA II (Beijing)
Fortrea(24 days ago)
About this role
This role involves managing and monitoring clinical trial sites to ensure compliance with regulatory guidelines and study protocols. It includes coordinating site activities, verifying data integrity, and ensuring participant safety, all within a structured clinical research environment.
Required Skills
- ICH GCP
- Clinical Monitoring
- Source Data Verification
- Regulatory Compliance
- Study Management
- eCRF
- Data Review
- SAE Reporting
- Trial Management Systems
- Site Management
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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