FSP CRA I (Jinan)
Fortrea(27 days ago)
About this role
This role involves overseeing site management and monitoring for clinical studies, ensuring compliance with regulatory standards and project plans. The job requires collaborating with study staff, managing resources, and maintaining data integrity to facilitate successful clinical research operations.
Required Skills
- Clinical Monitoring
- Data Management
- Regulatory Compliance
- Protocol Adherence
- CRF Review
- Investigator Liaison
- Trial Management
- GCP
- Clinical Operations
- Study Coordination
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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