FSO CRA(Shenyang/Zhengzhou/Changchun)
Fortrea(2 months ago)
About this role
A Clinical Research Associate at Fortrea supports the conduct and oversight of clinical studies, ensuring adherence to company SOPs, ICH GCP, and applicable regulatory requirements. The role focuses on protecting study subjects, safeguarding data integrity, maintaining regulatory and sponsor documentation, and supporting audit readiness while collaborating with study teams and sponsors.
Required Skills
- Site Management
- Clinical Monitoring
- Source Verification
- Regulatory Compliance
- GCP Knowledge
- eCRF Review
- CTMS
- SAE Reporting
- Data Integrity
- Audit Readiness
+2 more
Qualifications
- University or College 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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