FSP CRA II（Wuhan）
Fortrea(2 months ago)
About this role
A Clinical Research Associate responsible for site management and monitoring of clinical trials to ensure compliance with Fortrea SOPs, ICH GCP, and sponsor/regulatory requirements. The role includes conducting pre-study, initiation, routine, and close-out visits, source document verification, eCRF review, and management of investigational product accountability. The position requires frequent travel to study sites (approximately 60%) and collaboration with study teams to maintain data integrity and audit readiness.
Required Skills
- Clinical Monitoring
- Site Management
- Source Verification
- Regulatory Compliance
- eCRF Review
- CTMS
- IP Accountability
- SAE Tracking
- Monitoring Plans
- Communication
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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