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Research Study Start-Up Coordinator

Dartmouth Health • Lebanon, NH, US • published 2026-11-09 07:00:06.302353

Description

**Overview**Responsible for managing the startup activities of clinical trials. Collaborates with internal and external stakeholders with responsibility for protocol activation in alignment with departmental and D\-HH goals. Serves as the primary responsible party and point of contact during clinical research trial feasibility, planning, and implementation stages up until the point of site activation. **Responsibilities*** Organizes and manages implementation of activities required for the study activation process, including, but not limited to feasibility, committee approvals, and regulatory information. * Leads study site selection and start\-up activities. * Responsible for tracking progress of all studies in the department activation pipeline and meets with the research teams to review the studies’ progress and determine plan of action to ensure study startup is not delayed. * Meets with Regulatory team to review progress of committee submissions. * Coordinates and attends all Resource Meetings held with the Clinical Trials Office and study team members. Ensures follow\-up action items are progressing in a timely manner. * May assist with the determination of department personn...

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