Job Description
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).
Job Tags
Contract work,