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# Research Assistant - Data Coordinator

- **Company:** Dartmouth Health
- **Location:** Lebanon, NH, United States (Remote available)
- **Contract:** Permanent contract
- **Skills:** Clinical Trial Management Systems, Data Integrity, Electronic Data Capture, Electronic Medical Records
- **Published:** July 11, 2026
- **Apply:** https://dejobs.org/x/x/64622A5BDF544B1CAF06AA1AF2B801D6/job/

## About the Role

+ High School or equivalent required
*

 + Associates degree preferred
*

 + Previous research experience preferred

## Description

The Research Assistant works closely with other research staff and supports data entry for clinical trials. The Research Assistant has no supervisory responsibilities and works under direct supervision a supervisor of research programs, a research operations manager, or an education program manager. They cannot perform any tasks that by state or local law require a license to perform., * Primarily supports subject management, such as, performs data entry in the Clinical Trial Management System (CTMS) and supports data entry needs of the study.

 * Adheres to the principles for the ethical conduct of research, and safeguards for protection of human subjects especially when conducting research with vulnerable populations.
 * Understands and prioritizes the safety of research participants.
 * Utilizes Electronic Data Capture (EDC) systems, technologies and software necessary for study operations.
 * Completes data entry related to test results and/or measures according to protocol, and appropriate to role. Completes electronic Case Report Forms (eCRFs) accurately and according to protocol.
 * Assists with investigating incomplete, inaccurate or missing data and or documents to ensure accuracy and completeness of data; follows Standard Operating Procedures (SOPs) for data quality assurance.
 * Appropriately utilizes standard processes, policies and systems to ensure data integrity, attribution, and security.
 * Follow patients for the duration of study participation via electronic medical record review to ensure protocol compliance
 * Complete data entry as required for individual study protocols ensuring compliance with institutional and regulatory requirements.
 * Monitor and report adverse events and deviations as required by the sponsor, institution, and federal regulations
 * Ensure adequate source documentation is in place for all data reported
 * Resolve data queries issued by the sponsor
 * Obtain protocol clarifications from the study sponsor and communicate information to the research team
 * Schedule and prepare for monitoring visits with sponsors
 * Facilitate the request and shipment of archival pathology samples
 * Organize and prepare for internal and external audits
 * Maintain ongoing communication with clinical team regarding study patients and progress for multiple studies
 * Understand and demonstrates the professional guidelines and code of ethics related to the conduct of clinical research.
 * Completes all D-H and project-specific training requirements.
 * Communicates appropriately (written and orally) between stakeholders.
 * Assists with communications between principal investigators, regulatory agencies, D-H stakeholders and study participants to resolve problems.
 * Performs other duties as required or assigned.


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