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CLINICAL TRIALS STUDY COORDINATOR

None • Fort Gratiot Township, MI, US • published 2026-09-30 01:58:36.372707

Description

We are seeking a **Full Time,** **Mon\-Thurs,** **on\-site** Clinical Trials Study Coordinator for our Canton and Ann Arbor locations. Must be willing to travel to both locations. Mon and Tues will be at our Ann Arbor location, Wed and Thurs at our Canton location. **Summary:** The Clinical Research Coordinator is responsible for managing clinical trial performance and ensuring the conduct of their clinical trials is congruent with the vision and mission of the company. The CRC plans, coordinates, evaluates, and manages the care of both the participants and the data for their assigned trials. The CRC follows study specific protocol guideline and communicates and interacts with Investigators, clinic staff, CROs and Sponsors to effectively perform clinical research and coordinate research activities. All duties carried out by the CRC are done so in accordance with company policies, SOPs, and Good Clinical Practice (GCP) as well as all applicable local, state and federal regulations. **Primary Responsibilities:** * Coordinate clinical trials conducted by a supervising Principal Investigator in accordance with FDA, GCP and protocol guidelines. * Identify potential problems or inconsist...

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