Talent.com
No longer accepting applications
Clinical Research Coordinator - 247699

Clinical Research Coordinator - 247699

MedixGreenville, SC, US
2 days ago
Job type
  • Temporary
Job description

Looking for a strong Clinical Research Coordinator to join our team!

  • This is a 6 month contract to hire (based off performance / attendance)
  • Must have Clinical Research Coordinator experience
  • Experience with weight loss, diabetes or endocrinology studies

Start Date : December 1st

100% onsite!!!

Clinical Trial Coordination

  • Coordinate and manage all aspects of assigned Phase 2–4 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 with 21 CFR Part 11, ICH GCP, and sponsor SOPs.

    • 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.

    • 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.

  • Provide on-site support at additional study locations when required (occasional travel).
    • Create a job alert for this search

    Clinical Research Coordinator • Greenville, SC, US