Job Description
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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