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Research Project Coordinator

Job in Hanover, Grafton County, New Hampshire, 03755, USA
Listing for: Inside Higher Ed
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
  • Research/Development
    Clinical Research, Research Scientist, Medical Science
Salary/Wage Range or Industry Benchmark: 53800 - 67300 USD Yearly USD 53800.00 67300.00 YEAR
Job Description & How to Apply Below

5 days ago Be among the first 25 applicants

Position Purpose

To support the Department of Epidemiology at the Geisel School of Medicine at Dartmouth in achieving its mission to conduct rigorously constructed research and apply state‑of‑the‑art and novel methods and technologies to advance the field of epidemiology and impact human health and disease. In collaboration with project leaders, the Research Project Coordinator will coordinate the implementation and ongoing activities for a large National Institute of Health (NIH) funded Environmental influences on Children’s Health Outcome (ECHO) birth cohort study.

Job

Details
  • Posting Date: 12/19/2025
  • Open Until Filled:
    Yes
  • Position Number: 1129504
  • Position Title:

    Research Project Coordinator
  • Hiring Range Minimum: $53,800
  • Hiring Range Maximum: $67,300
  • Union Type:
    Not a Union Position
  • SEIU Level: Not an SEIU Position
  • FLSA Status:
    Exempt
  • Employment Category:
    Regular Full Time
  • Scheduled Months Per Year: 12
  • Scheduled Hours Per Week: 40
  • Location:

    Lebanon, NH
  • Remote Work Eligibility:
    Onsite only
  • Term Position:
    No
  • Grant Funded Position:
    Yes
Recruitment, Interviewing and Measurement/Specimen Collection
  • Responsible for recruitment/enrollment of study participants remotely and/or in person.
  • Coordinates, schedules, and completes recruitment activities using established study protocols.
  • Implements the research activities including distribution and completion of surveys, data collection and management, subject identification, recruitment, interviewing, and scheduling.
  • Maintains a high level of research professionalism to maintain participant engagement and retention.
  • Provides education and instruction to participants on informed consent, study materials, collection of samples, measurements, and follow‑up processes according to protocols.
  • Conducts necessary follow‑up activities as needed and coordinates with laboratory and other study personnel to ensure specimens and measurements are collected, processed, entered into databases, and delivered according to protocol.
  • Enter accurate study data in established databases in a timely manner according to protocols.
Coordination
  • Works closely with the principal investigator and research directors on the development of, revisions and updates to protocols, study materials, and supplies.
  • Maintains close communication with the principal investigator, study research directors, and other study staff regarding study progress, processes, and the collection and delivery of samples.
  • Assists study research directors with data monitoring and tracking activities, preparation of reports, Institutional Review Board (IRB) renewals and revisions, and coordination of other administrative activities as needed.
  • Coordinates collection and delivery of samples with laboratory, clinics, hospital staff, and other study staff as needed.
  • Maintains study supplies, equipment, and materials.
Medical Records
  • May conduct medical record reviews according to study protocols and may act as a clinical resource to other study staff for medical record reviews.
  • Maintains working relationships with medical and administrative staff to coordinate medical record review activities.
Data Management
  • Ensures that data are successfully collected and managed.
  • Ensures that subject and data confidentiality is maintained, and data integrity is maintained.
  • Generates pertinent reports on a monthly or as‑needed basis. Assists in the organization of study‑related protocols on the server.
Project Support
  • Coordinates periodic review and update of protocols and assists in preparation of materials for IRB requests and renewals.
  • Maintains accurate and efficient tracking system for study documents approved by IRB and assures protocol materials are up to date and distributed appropriately.
  • Coordinates mailings for study subjects, follows up with staff on missing forms and materials, and maintains a supply of materials for staff.
Miscellaneous
  • Other study tasks as needed
  • Adheres to the most current public health recommendations regarding COVID-19, including symptom surveillance, screening questions, and personal protective equipment.
Required Qualifications
  • Bachelor’s degree in health or social sciences, or the equivalent…
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