Clinical research nurse coordinator · What it does
Three tasks it takes off your hands
- Schedule subjects for appointments and procedures as required by study protocols.
- Prepare study-related documentation such as protocol worksheets and adverse event reports.
- Oversee subject enrollment to ensure informed consent is properly obtained and documented.
Where these come from
The tasks of “Clinical Research Coordinators” (O*NET 11-9121.01), as O*NET lists them:
- Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
- Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
- Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
