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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.

Primary Directive

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

Execution Steps
  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.

Toolbox Requirements
IBM SPSS StatisticsMicrosoft AccessMicrosoft ExcelMicrosoft Office softwareMicrosoft OutlookMicrosoft PowerPointMicrosoft ProjectMicrosoft WordPythonRSASThe MathWorks MATLAB

Free — no credit card required. 200 messages included.