Clinical Research Associate

VirtualVocations

Springfield, OHFull-timePosted Apr 14, 2026

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Job Description

achelor's degree in life sciences, nursing, or a related field; advanced degree preferred

Minimum of 3+ years of clinical operations experience in biotech, pharma, or CRO environments

Prior experience in site management and CRO oversight strongly preferred

Strong knowledge of ICH-GCP, FDA regulations, and global clinical trial requirements

Experience with EDC systems, CTMS, eTMF, and safety reporting processes

Qualifications

  • •Minimum of 3+ years of clinical operations experience in biotech, pharma, or CRO environments
  • •Strong knowledge of ICH-GCP, FDA regulations, and global clinical trial requirements
  • •Experience with EDC systems, CTMS, eTMF, and safety reporting processes

Benefits

    Responsibilities

    • •Support site initiation, ongoing management, and close-out activities in accordance with study timelines
    • •Ensure compliance with study protocol, ICH-GCP, FDA regulations, and company SOPs
    • •Provide oversight of CRO CRAs and site management activities, and maintain a compliant Trial Master File
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