FSP CRA(Tianjin)
Fortrea(1 month ago)
About this role
A Clinical Research Associate at Fortrea supports clinical studies by ensuring study conduct aligns with protocols, regulatory and sponsor requirements, and global quality standards. The role interfaces with study sites and internal teams to maintain regulatory documentation, data integrity, and audit readiness throughout the trial lifecycle.
Required Skills
- Site Monitoring
- Source Verification
- eCRF Review
- Regulatory Compliance
- ICH GCP
- SAE Reporting
- CTMS
- Trial Management
- Data Integrity
- Patient Safety
Qualifications
- University Degree
- Allied Health Certification
- Nursing Licensure
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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