Looking for a strong Clinical Research Coordinator to join our team!
- This is a 6 month contract to hire (based off performance / attendance)
- Must have Clinical Research Coordinator experience
- Experience with weight loss, diabetes or endocrinology studies
Start Date : December 1st
100% onsite!!!
Clinical Trial Coordination
Coordinate and manage all aspects of assigned Phase 24 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).