FSP CRA II (Beijing/Harbin/Changchun)
Fortrea(27 days ago)
About this role
This role involves site management and monitoring responsibilities for clinical studies, ensuring compliance with regulatory standards, safeguarding data integrity, and supporting clinical trial operations. The position includes travel to study sites and collaboration with study teams to meet project goals.
Required Skills
- GCP
- Monitoring
- Regulatory Compliance
- Clinical Trials
- Data Review
- Source Documentation
- eCRF
- SAE Reporting
- Project Management
- Clinical Operations
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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