FSP CRA II
Fortrea(4 days ago)
About this role
Fortrea is looking for experienced Clinical Monitors to oversee and manage clinical studies at research sites, ensuring adherence to regulations and protocol standards. The role involves site management, data verification, and collaboration with study teams, with a focus on quality and compliance in clinical trial processes.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Source Document Review
- eCRF
- Data Management
- Regulatory Documentation
- SAE Reporting
- Clinical Trials
- Project 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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