Clinical Research Coordinator

4 weeks ago

Greenville SC, United States Medix™ Full time

Looking for a strong Clinical Research Coordinator to join our team
Must have:
~1 year of Clinical Research Coordinator experience
~2 years of Phlebotomy experience
~ Experience with one of the following (Endocrinology, Diabetes or weight loss)
~ GLP experience


Estimated Duration of Assignment: 6 month contract with the possibility to be hired on permanently depending on company needs/performance


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).

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