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Clinical Research Coordinator I

Dartmouth Health • Lebanon, NH, US • published 2026-11-09 07:00:06.302051

Description

**Overview**Clinical Research Coordinator I works closely with other research staff and is involved at a fundamental level to support basic administrative clinical trial tasks. The Clinical Research Coordinator I has no supervisory responsibilities and works under direct supervision of the Principal Investigator or designee. They cannot perform any tasks that by state or local law require a license to perform. **Responsibilities*** Research Operations * May arrange/schedule required appointments. * Learns and supports all of aspects of the study operations (subject management/regulatory) with substantial oversight from the investigator or their designee. * Primarily supports subject management, such as subject visit preparation, performs data entry in the Clinical Trial Management System (CTMS), scans informed consents into Electronic Medical Record (EMR) and supports data entry needs of the study. * Regulatory Affairs * Assists with compiling and maintaining essential records and documents required by Dartmouth\-Hitchcock Medical Center (DHMC) and various sponsor organizations in compliance with applicable standards operating procedures for the execution of clinical trial operatio...

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