Clinical Research Coordinator - 247690
MedixMemphis, TN, US1 day ago
Job type
- Full-time
- Temporary
Job descriptionCoordinate 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). 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. 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. Serve as the primary point of contact for sponsors, CROs, monitors, and other site staff. Provide on-site support at additional study locations when required (occasional travel).
Looking for a strong Clinical Research Coordinator to join our team!
Must have :
- Patient Facing experience
- Phlebotomy experience
- Experience with Endocrinology, Diabetes or Weight Loss
- 2 years of Clinical Research Coordinator experience
Comfortable with a 6 month contract to hire (based off performance / attendance and company needs.
100% onsite full-time 40 hours a week Monday - Friday
Clinical Trial Coordination
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 • Memphis, TN, US
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