Clinical Research Coordinator 247698 (Cary)Medix • Cary, NC, US
Clinical Research Coordinator 247698 (Cary)
Medix • Cary, NC, US
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job_description.job_card.job_descriptionUtilize eSource, eConsent, eISF, and other clinical trial software platforms to maintain complete, accurate, and regulatory-compliant study records. Support site readiness and 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. 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 Serve as the primary point of contact for sponsors, CROs, monitors, and other site staff.
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
Regulatory Compliance
Patient Engagement & Safety
Collaboration & Support
Support training and mentoring of new CRC staff as assigned.
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Clinical Research Coordinator • Cary, NC, US
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