Roles · Science and research

AI clinical research manager

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

Losa Murphy“I prepare study documentation and monitor compliance.”An example character, not a real person.
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Clinical research manager · 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.
  3. Monitor study activities to ensure compliance with protocols.
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.
  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.

Clinical research manager · 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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