Clinical Research Coordinator 246208

Clinical Trial Coordination & Execution

Manage all phases of clinical trials from initiation to close-out. Conduct study visits, obtain informed consent, perform protocol procedures, and enter data accurately into eCRFs using eSource systems.

Technology & Compliance

Utilize clinical trial platforms (eSource, eConsent, eISF) to maintain regulatory-compliant documentation. Ensure site adherence to 21 CFR Part 11, ICH GCP, and sponsor SOPs.

Regulatory & Audit Readiness

Maintain regulatory documentation and assist in audit preparation for sponsors, CROs, and regulatory agencies.

Patient Engagement & Safety

Recruit, screen, and enroll participants per protocol; monitor and report adverse events to ensure patient safety.

Collaboration & Site Support

Act as liaison with sponsors, CROs, and monitors. Mentor new CRCs and provide on-site support or travel as needed for multi-site coordination, audits, or meetings.