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Clinical Research Coordinator

Be Well Clinical Studies • Lincoln, NE, US • published 2026-10-23 02:05:07.169515

Description

Be Well Clinical Studies is seeking a detail\-oriented and patient\-centered **Clinical Research Coordinator (CRC)** to manage and execute clinical research studies at our Lincoln site. This role serves as a primary operational lead on assigned protocols, ensuring studies are conducted in accordance with sponsor requirements, FDA regulations, and Good Clinical Practice (GCP) standards. The CRC works closely with the Principal Investigator (PI), sub\-investigators, Clinical Operations Manager, and cross\-functional research teams to ensure study integrity, subject safety, and high\-quality data collection. **Key Responsibilities** **Study Coordination \& Compliance** * Manage day\-to\-day study operations in accordance with protocol, GCP, and regulatory requirements * Maintain Investigator Site Files (ISF) and study documentation in electronic systems (CRIO, sponsor portals) * Ensure protocol adherence and support audit/monitoring readiness **Participant Care \& Safety** * Conduct and document the informed consent process * Perform subject visit coordination including scheduling, follow\-ups, and visit flow management * Collect medical history, medication history, and demographic da...

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