FSP CRA II (Shanghai)
Fortrea(1 month ago)
About this role
A Clinical Research Associate at Fortrea supports the conduct and quality oversight of clinical trials across multiple study sites. The role ensures compliance with regulatory standards and Good Clinical Practice while interfacing with study teams and investigators. The position requires substantial travel and may serve as a Lead CRA on assigned projects.
Required Skills
- Site Monitoring
- Source Verification
- Regulatory Compliance
- ICH GCP
- eCRF Review
- Data Management
- SAE Reporting
- Site Management
- Project Planning
- CTMS
+3 more
Qualifications
- University Degree
- Certification in Allied Health
- 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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