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Clinical Research Coordinator 247698 (Cary)
Clinical Research Coordinator 247698 (Cary)Medix • Cary, NC, US
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Clinical Research Coordinator 247698 (Cary)

Clinical Research Coordinator 247698 (Cary)

Medix • Cary, NC, US
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Clinical Trial Coordination

  • Coordinate and manage all aspects of assigned clinical trials from site initiation to close-out.
  • Conduct study visits, including obtaining informed consent, performing protocol-required procedures, and collecting source data using eSource systems.
  • Ensure timely and accurate entry of study data into electronic case report forms (eCRFs).

Technology & Documentation

  • Utilize eSource, eConsent, eISF, and other clinical trial software platforms to maintain complete, accurate, and regulatory-compliant study records.
  • Support site readiness and compliance

    • Regulatory Compliance

  • Maintain up-to-date regulatory documents and study binders (electronic and / or paper as required).
  • Assist with preparation for sponsor, CRO, or regulatory audits.

    • Patient Engagement & Safety

  • Recruit, screen, and enroll study participants according to protocol inclusion / exclusion criteria.
  • Ensure ongoing patient safety by monitoring for adverse events and reporting per protocol.
  • Execute phlebotomy

    • Collaboration & Support

  • Serve as the primary point of contact for sponsors, CROs, monitors, and other site staff.

    • Support training and mentoring of new CRC staff as assigned.

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    Clinical Research Coordinator • Cary, NC, US

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