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U.S. Dept. of Labor code 11-9121.01Market Standard — pending BLS/OEWS enrichment

Clinical Research Coordinators

Plan, direct, or coordinate clinical research projects. Direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. May evaluate and analyze clinical data.

What this job is about

Facilitate and oversee clinical research studies ensuring compliance and data integrity.

What this work involves, step by step

AI can help most with the planning, drafting, and paperwork below — not the hands-on parts.

  1. 1

    Schedule subject appointments

    Coordinate and schedule subjects for necessary appointments as per study protocols.

  2. 2

    Assess subject eligibility

    Evaluate potential subjects through interviews and medical record reviews to determine eligibility.

  3. 3

    Prepare study documentation

    Create and maintain essential study-related documents including protocol worksheets and progress reports.

  4. 4

    Monitor study compliance

    Ensure all study activities adhere to protocols and regulatory requirements throughout the research.

  5. 5

    Record and report adverse events

    Document any adverse events and collaborate with investigators for proper reporting to oversight agencies.

Tools used in this work
IBM SPSS StatisticsMicrosoft AccessMicrosoft ExcelMicrosoft Office softwareMicrosoft OutlookMicrosoft PowerPointMicrosoft ProjectMicrosoft WordPythonRSASThe MathWorks MATLAB

Free — no credit card required. 200 messages included.