FSP CRA II (Shanghai)
Fortrea(21 days ago)
About this role
A Clinical Research Associate at Fortrea oversees the management and monitoring of clinical studies to ensure compliance with regulatory standards, data integrity, and subject protection. The role involves site visits, data verification, and collaboration with study teams to ensure study milestones are met.
Required Skills
- GCP
- FDA
- Clinical Monitoring
- Source Data Verification
- Regulatory Compliance
- eCRF
- Clinical Trials
- Investigator Management
- Study Planning
- Data 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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