Sr Clinical Research Associate
About the role
This opportunity puts you at the center of site oversight, data integrity, and cross-functional collaboration—driving research forward where it matters most.
Responsibilities
- Oversee site feasibility, selection, initiation, monitoring, and close-out activities
- Ensure data quality through source data verification and site compliance
- Partner with vendors, investigators, and project teams to resolve issues
- Track enrollment, protocol deviations, and monitoring metrics
- Support study planning, training, and electronic system development
Requirements
- Bachelor’s degree, preferably in life sciences
- Strong knowledge of U.S. regulatory requirements and ICH-GCP
- Proficient with EDC, CTMS, and Microsoft Office tools
- Highly organized with exceptional communication skills
- Comfortable working independently in a remote, fast-paced environment
Qualifications
Competitive Salary and Bonus
Awesome Benefits and tons of opportunity for growth
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