FSP CRA I (Beijing)
Fortrea(29 days ago)
About this role
A Clinical Research Associate (CRA) is responsible for site management and monitoring for clinical studies, ensuring compliance with regulatory and company standards. They oversee the study process at local sites, maintain communication with vendors and stakeholders, and ensure data integrity and patient safety.
Required Skills
- GCP
- CRF Review
- Site Management
- Regulatory Guidelines
- Clinical Monitoring
- Data Management
- Good Communication
- Study Coordination
- Quality Control
- Clinical Trials
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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