California Licensed Clinical Trials Coordinator

Virtual Vocations Inc

Cedar Rapids, IAFull-timePosted Apr 12, 2026

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Job Description

 research staff

Required Qualifications

Bachelor's degree in Science, Health, or a related field, or equivalent relevant work experience
Minimum of 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), Electronic Medical Records (EMR), and eRegulatory systems

Qualifications

  • •Bachelor's degree in Science, Health, or a related field, or equivalent relevant work experience
  • •Minimum of 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), Electronic Medical Records (EMR), and eRegulatory systems

Benefits

    Responsibilities

    • •Coordinate data collection, entry, quality assurance, and query resolution for oncology clinical trials
    • •Ensure regulatory compliance and data accuracy through quality checks and timely resolution of discrepancies
    • •Support monitoring visits, audits, and contribute to data management improvements and training of research staff
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