Roles · Science and research

AI clinical program coordinator

Plans and coordinates clinical research projects. Directs activities to ensure compliance with protocols and objectives. Evaluates and analyses clinical data.

Lauren Moreau“I prepare documentation and record adverse event data.”An example character, not a real person.
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Clinical program coordinator · What it does

Three tasks it takes off your hands

  1. Prepare study-related documentation such as protocol worksheets and reports.
  2. Record adverse event and side effect data for reporting.
  3. Oversee subject enrollment to ensure informed consent is documented.
Where these come from

The tasks of “Clinical Research Coordinators” (O*NET 11-9121.01), as O*NET lists them:

  • Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
  • Oversee subject enrollment to ensure that informed consent is properly obtained and documented.

Clinical program coordinator · Tools and industries

It works in the tools you already use

  • Microsoft Excel
  • Microsoft Office software
  • Microsoft PowerPoint
  • IBM SPSS Statistics
  • Microsoft Access
  • Microsoft Outlook

Industries it fits

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Role facts from O*NET 31.0 Database (U.S. Department of Labor, Employment and Training Administration (USDOL/ETA), CC BY 4.0), written in our words. Sources and credits

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