Clinical Research Assistant supporting studies to improve outcomes for brain tumor patients at Duke Cancer Institute. Engaging in participant interactions and managing clinical trial operations with care and precision.
Responsibilities
Screen and consent participants for minimal risk studies, ensuring proper documentation and ethical compliance
Coordinate and schedule study visits, prepare necessary materials, and support participant interviews
Collect and manage biological specimens, maintain inventory, and ensure proper handling and shipping procedures
Enter and verify clinical data using EDC systems, run reports, and ensure data accuracy and completeness
Collaborate and communicate with study personnel to resolve routine issues and support study implementation
Participate actively in team meetings, committees, and continuing education opportunities
Uphold ethical standards in research, especially when working with vulnerable populations, and ensure participant safety
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