University of Vermont Health Network·Burlington, Vermont
The coordinator implements and manages clinical and non-clinical tasks to ensure the successful completion of research protocols. The role involves coordinating activities within the Trauma and Critical Care department.
The Clinical Research Coordinator I coordinates and implements vital clinical and non-clinical tasks to the successful completion of one or more research protocols consistent with knowledge and experience. A successful Clinical Research Coordinator I requires specialized knowledge and skills that are acquired through experience and/or education. This position should be extramurally funded therefore continued employment is largely dependent on the availability of funds in addition to satisfactory performance. EDUCATION: Associates Degree required or equivalent technical certification (e.g., EMT, EKG Technician, Medical Assistant). Bachelor degree preferred. EXPERIENCE: No prior research experience necessary. Some experience in a clinical setting is preferred, but not required unless the candidate does not have an Associates Degree. This is a grant funded position.This is a bargaining union position.
An Associate degree or equivalent technical certification is required, while a Bachelor's degree is preferred. No prior research experience is necessary, though clinical experience is preferred.
Market context
Clinical Research Coordinator I roles in Vermont are often tied to hospital-based studies and can draw interest from candidates with clinical backgrounds, especially when no prior research experience is required. These positions can be competitive because employers may prefer applicants who can work with patients, follow protocols closely, and handle documentation in fast-paced trauma and critical care settings. Review the AI-summarized requirements and benefits on this platform to save time, and tailor your application to any direct patient-care, coordination, or compliance experience.
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