FSO - CRA II (Wuhan)
Fortrea(1 month ago)
About this role
A Clinical Research Associate at Fortrea supports clinical studies by ensuring site compliance with regulatory standards, data integrity, and study documentation. The role works within Fortrea SOPs and ICH GCP guidelines, engages with study teams and sponsors, and requires significant travel to study sites.
Required Skills
- Site Monitoring
- Source Verification
- ICH GCP
- Regulatory Compliance
- eCRF Review
- CTMS
- SAE Reporting
- IP Accountability
- Data Integrity
- Microsoft Office
+5 more
Qualifications
- University Degree
- Allied Health Certification
- Nursing License
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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