Roles · Science and research

AI clinical trial manager

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

Leah Dubois“I prepare study documentation and record adverse event data for investigators.”An example character, not a real person.
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Clinical trial manager · What it does

Three tasks it takes off your hands

  1. Prepare study-related documentation such as protocol worksheets and adverse event reports.
  2. Record adverse event and side effect data and confer with investigators.
  3. Oversee subject enrollment to ensure that informed consent is properly obtained.
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 trial 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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