Principal Clinical Research Coordinator

VirtualVocations

Livonia, MIFull-timePosted Apr 1, 2026

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Job Description

aining, and Education

Bachelor's degree in science, health, or a related field from an accredited university

5-7 years of research or relevant experience

Experience with CTMS, EMR, and eRegulatory Systems

Working knowledge of clinical trials and relevant regulations

Good Clinical Practice (GCP) and Human Subjects Protection (HSP) certifications required within specified timeframes

Qualifications

  • •Bachelor's degree in science, health, or a related field from an accredited university
  • •5-7 years of research or relevant experience
  • •Experience with CTMS, EMR, and eRegulatory Systems
  • •Working knowledge of clinical trials and relevant regulations
  • •Good Clinical Practice (GCP) and Human Subjects Protection (HSP) certifications required within specified timeframes

Benefits

    Responsibilities

    • •Serve as the primary point of contact between study sponsors, investigators, and research teams
    • •Oversee operational execution of studies, including patient registration and study close-out activities
    • •Ensure regulatory compliance and accurate documentation across various systems
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