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Clinical Research Coordinator 1

AMR Clinical • Lexington, KY, US • published 2026-09-26 09:51:26.213629

Description

The Clinical Research Coordinator will perform and manage tasks that are critical to clinical research studies. The Clinical Research Coordinator must ensure compliance with federal regulations, study protocol guidelines, as well as monitor study participants, and take a proactive approach to identify issues on an ongoing basis throughout the clinical research study. *To consistently embody AMR Clinical’s Core Values:* * *United We Achieve* * *Celebrate Diverse Perspectives* * *Do the Right Thing* * *Adapt and Persevere* The Clinical Research Coordinator reports to the Site Manager/Team Lead. Classification: Non\-Exempt **Primary** **Responsibilities:** * Focuses on compliance responsibilities, including protocol deviations, SAE reporting, and informed consent. Strong focus on compliance responsibilities, including managing protocol deviations, SAE reporting, and ensuring proper informed consent procedures. * Coordinate clinical trials per FDA requirements and GCP Guidelines per sponsor protocols. * Manage and document Adverse Event and Serious Adverse Event reporting in compliance with FDA, IRB, and sponsor requirements, ensuring timely follow\-up and resolution. * Establish under...

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