FSP CRA II (Beijing)
Fortrea(1 month ago)
About this role
A Clinical Research Associate (CRA) at Fortrea supports the conduct of clinical trials by ensuring sites adhere to regulatory standards and study requirements. The role is part of the clinical operations team, requiring clinical research experience, regulatory knowledge, and frequent travel to investigator sites. It contributes to study quality, data integrity, and audit readiness across assigned projects.
Required Skills
- Site Monitoring
- GCP
- Regulatory Compliance
- Source Verification
- Data Review
- eCRF
- CTMS
- SAE Reporting
- Clinical Trials
- 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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