FSP CRA I
Fortrea(3 days ago)
Guangzhou, GuangdongOnsiteFull TimeJunior$43,063 - $58,543 (estimated)Clinical Operations
Apply NowAbout this role
A Clinical Research Associate at Fortrea is responsible for site monitoring and management of clinical studies, ensuring regulatory compliance, data integrity, and patient safety. The role involves working closely with trial sites, vendors, and internal teams to support the successful execution of clinical trials.
Required Skills
- GCP
- CRF
- Regulatory Guidelines
- Clinical Trials
- Site Management
- Data Review
- Monitoring
- Protocol Compliance
- Study Coordination
- CTMS
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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