FSP CRA II（Shanghai）
Fortrea(1 month ago)
About this role
A Clinical Research Associate (CRA) at Fortrea provides field-based monitoring support for clinical trials to ensure studies are conducted in compliance with regulatory and sponsor requirements. The role supports study documentation, site readiness, and coordination with cross-functional study teams while spending substantial time on site visits.
Required Skills
- Site Monitoring
- ICH GCP
- Regulatory Compliance
- Source Verification
- eCRF Review
- CTMS
- SAE Reporting
- IP Accountability
- Audit Readiness
- Project Planning
+3 more
Qualifications
- University Degree
- 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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