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Research Assistant

AMR Clinical • Lexington, KY, US • published 2026-09-25 05:23:59.561931

Description

The role of the Research Assistant is responsible for performing a wide variety of administrative and clinical tasks to support the study site. The Research Assistant supports all study related activities to ensure that the study is completed accurately per study protocol. The Research Assistant is an integral role to assist with the flow of the clinic. *To consistently embody AMR Clinical’s Core Values:* * *United We Achieve* * *Celebrate Diverse Perspectives* * *Do the Right Thing* * *Adapt and Persevere* The Research Assistant reports to the Site Manager/Team Lead. Classification: Non\-Exempt **Primary Responsibilities:** * Effectively prioritize tasks and meet deadlines in a fast\-paced environment. * Maintain a strong emphasis on compliance responsibilities, including timely identification and reporting of protocol deviations, serious adverse events (SAEs), and adherence to regulatory and site\-specific requirements. * Monitor \& Report Adverse Events – Recognize and promptly report AEs, protocol deviations, and safety concerns to the clinical team. Document AEs and Serious Adverse Event reporting in compliance with FDA, IRB, and sponsor requirements, ensuring timely follow\-u...

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