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Clinical Research Coordinator I

Alliance Clinical Network • West Hills, CA, US • published 2026-09-29 08:55:30.955055

Description

**Summary:** The Clinical Research Coordinator I (CRC) supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. This role involves direct interaction with participants including monitoring the health of each participant throughout the trial. The CRC plays a key part in maintaining study integrity and quality and collaborating with the Principal Investigator (PI) to provide oversight of the study to ensure adherence to Good Clinical Practice (GCP) guidelines. **Essential Duties and Responsibilities:** * Communicate clearly and professionally with study participants regarding study objectives and ongoing instructions. * Adhere to site standard operating procedures (SOPs). * Administer questionnaires and monitor participant compliance with study protocols. * Respond to participant needs promptly and appropriately. * Collect and document patient medical history and health conditions. * Obtain and document informed consent from study participants. * Maintain accurate records of investigational product (IP) dispensation and accountability. * Coordinate with laboratories to ensure time...

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