Clinical Trial Central Screener
Sarah Cannon Research InstituteKnoxville, Tennessee, United States
Posted May 11, 2026
Full Time
About the Company
Sarah Cannon Research Institute is one of the world’s leading oncology research organizations conducting community-based clinical trials.
Job Description
Clinical Trial Central Screener role at Sarah Cannon Research Institute, responsible for patient screening, data analysis, and communication with site personnel. The role requires a bachelor's degree in nursing or a licensed registered nurse, with 3+ years of experience in clinical research and experience in clinical trials.
Requirements
- Clinical support for clinical trial central screening process
- Serve as a liaison between SCRI network sites and Personalized Medicine Operations team
- Aid in the enhancement of SCRI's precision medicine software platform, Genospace
- Escalate appropriate issues to supervisor
- Support the deployment, training, and utilization of Genospace at SCRI network sites
- Lead and facilite routine internal and external cross-functional meetings
- Build and maintain strategic relationships across the organization
Benefits
- Comprehensive benefits to support physical, mental, and financial well-being
- Competitive compensation package
- Annual bonus or long-term incentive opportunities
- 401k Matching
- Retirement Plan
