Clinical Research Coordinator II or III (CRC 2-3)

Role Overview: The Clinical Research Coordinator II or III is responsible for managing clinical research activities under the supervision of investigators, ensuring protocol compliance, and maintaining regulatory standards. Key Responsibilities: Coordinate and implement clinical protocols, collect and record data, assist in patient assessments, recruit and screen participants, and manage study documentation. Handle adverse event reporting, oversee study supplies, and perform tasks such as phlebotomy, vital signs, and patient education. Ensure accurate data entry, maintain source documentation, and support quality audits and inspections. Supervise support staff, mentor new hires, and serve as a liaison among physicians, vendors, and regulatory bodies. Qualifications & Skills: Minimum of 2 years’ experience in late-phase clinical trials, with knowledge of GCP, FDA regulations, and research ethics. Requires associate or bachelor’s degree in healthcare or related field, GCP certification, and familiarity with data management. Strong communication skills and ability to perform clinical procedures are essential. Additional Details: May involve some interoffice travel using company resources. Offers benefits including health plans, PTO, 401K, and educational support. Ensures compliance with equal employment opportunity policies.