Clin Res Assoc I
Fortrea(3 months ago)
About this role
A Clinical Research Associate / Site Manager responsible for supporting clinical study site oversight and ensuring studies align with company, sponsor, and regulatory standards. The role involves implementing assigned project plans, maintaining study documentation, and coordinating with sponsors, sites, and internal teams. Travel to investigator sites is required to support study activities and regulatory compliance.
Required Skills
- Site Monitoring
- Site Management
- Regulatory Guidelines
- Informed Consent
- Data Management
- CRF Review
- SAE Tracking
- Audit Readiness
- Project Coordination
- Vendor Management
+2 more
Qualifications
- University Degree
- Nursing Licensure
- Driver's License
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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