Sr CRA I
Fortrea(1 year ago)
About this role
A Senior Clinical Research Associate I at Fortrea conducts site monitoring and management for clinical studies, ensuring adherence to regulatory requirements and company SOPs. The role supports implementation of project plans, may serve as a Local Project Coordinator or Lead CRA, and contributes to trial documentation and coordination with investigators, vendors, and internal teams. The position requires frequent travel to study sites and engagement across global clinical development programs.
Required Skills
- Site Monitoring
- Site Management
- Regulatory Compliance
- SAE Reporting
- Data Review
- Project Coordination
- Communication
- Budget Negotiation
- Presentation Skills
- Training
Qualifications
- University Degree
- Life Science Degree Preferred
- Nursing Certification
- Medical Technology Certification
- Laboratory Technology Certification
- Valid Driver's License
- 3 Years Clinical Monitoring Experience
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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