FSP CRA II
Fortrea(1 month ago)
About this role
A Clinical Research Associate at Fortrea is responsible for managing and monitoring clinical study sites to ensure compliance with company SOPs, ICH GCP, and sponsor and regulatory requirements. The role focuses on protecting study subjects, ensuring data integrity, and maintaining regulatory documentation throughout the trial lifecycle. The position requires frequent travel to study sites and coordination with study teams to meet project timelines and deliverables.
Required Skills
- Site Monitoring
- Clinical Monitoring
- Source Verification
- Query Resolution
- Regulatory Compliance
- Informed Consent
- eTMF Management
- IP Accountability
- SAE Reporting
- CTMS
+2 more
Qualifications
- University Degree
- Certification In Allied Health
- Nursing Licensure
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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