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 complianceRegulatory 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 phlebotomyCollaboration & 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.