About this role
A Clinical Research Associate at Fortrea is responsible for overseeing clinical study site management, monitoring trial progress, ensuring regulatory compliance, and safeguarding data integrity. The role involves coordinating with study teams, managing site activities, and ensuring study protocols are followed to maintain high-quality standards in clinical trials.
Required Skills
- GCP
- SOPs
- Monitoring
- Regulatory Compliance
- Data Review
- eTMF
- SAE Reporting
- Clinical Trials
- Source Documentation
- Study Management
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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