FSP CRA II (Tianjin)
Fortrea(13 days ago)
About this role
A Clinical Research Associate at Fortrea is responsible for managing clinical studies at site level, ensuring compliance with regulatory guidelines, safeguarding data integrity, and supporting trial operations. The role involves site monitoring, regulatory documentation, training, and collaboration with study teams to ensure successful trial execution.
Required Skills
- ICH GCP
- Clinical Monitoring
- Source Data Verification
- Regulatory Documents
- eCRF
- Trial Management
- SAE Reporting
- Clinical Research
- Data Integrity
- Monitoring Procedures
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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