Senior Clinical Trials Data Coordinator

VirtualVocations

Denver, COFull-timePosted Mar 31, 2026

Behavioral Health Market Context

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Job Description

a staff

Required Qualifications

Bachelor's degree in Science, Health, or a related field, or equivalent relevant work experience

5-7 years of clinical research or related experience

Completion of Good Clinical Practice (GCP) and Human Subjects Protection (HSP) training within 1 month of employment

Ability to obtain SOCRA or ACRP certification within 2 years of employment

Experience with Clinical Trial Management Systems (CTMS) and Electronic Medical Records (EMR)

Qualifications

  • Bachelor's degree in Science, Health, or a related field, or equivalent relevant work experience
  • 5-7 years of clinical research or related experience
  • Completion of Good Clinical Practice (GCP) and Human Subjects Protection (HSP) training within 1 month of employment
  • Ability to obtain SOCRA or ACRP certification within 2 years of employment
  • Experience with Clinical Trial Management Systems (CTMS) and Electronic Medical Records (EMR)

Benefits

    Responsibilities

    • Coordinate data collection, entry, quality assurance, and query resolution for oncology clinical trials
    • Ensure data accuracy and compliance with regulatory guidelines while managing adverse event documentation
    • Support monitoring visits and contribute to data management improvements and training of research data staff


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