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Clinical Research Coordinator; Non-R.N

Job in Salt Lake City, Salt Lake County, Utah, 84193, USA
Listing for: University of Utah
Full Time, Seasonal/Temporary position
Listed on 2025-12-21
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research, Research Scientist
Salary/Wage Range or Industry Benchmark: 50000 - 65000 USD Yearly USD 50000.00 65000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Research Coordinator (Non-R.N.)

Clinical Research Coordinator (Non-R.N.)

Neuromechanics and Applied Locomotion Laboratory, University of Utah

Job Summary

The Neuromechanics and Applied Locomotion Laboratory at the University of Utah is hiring a Clinical Research Coordinator to assist with ongoing funded research examining balance and mobility, particularly in people with mild traumatic brain injuries (i.e., concussions). The candidate will work on several federally‑funded and foundation‑funded projects with Dr. Peter Fino and collaborators, interacting on a regular basis with volunteer research subjects, physical therapists, engineers, graduate students, postdoctoral fellows, and faculty from various campus departments, and with research teams across the country.

This position is patient‑sensitive and must fulfill all associated vaccination requirements, or be approved for an exemption, prior to the first day of work. We protect our patients, coworkers, and community by requiring all patient‑sensitive employees to be immunized according to CDC standards and hospital policy. Limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations.

Responsibilities
  • Oversee compliance to protocol; manage quality control, completion, and submission of study‑related documentation; prepare reports for organizations and agencies.
  • Monitor enrollment goals and initiate strategies to promote enrollment and participant compliance. Coordinate and perform responsibilities related to research participants, including determining subject population availability, developing informed consents and screening materials, screening and recruiting subjects, scheduling visits, obtaining informed consent, answering subject inquiries, collecting participant data, overseeing study visits, and acting as a point‑of‑contact between participants and study‑related parties.
  • Recognize, track, and report adverse events and protocol deviations.
  • Prepare for and coordinate site visits made by sponsors or federal agencies during the course and at the close of the study.
  • Represent the research program at meetings, national and international research consortia.
  • Prepare, submit, and maintain IRB, NIH, DOD, and/or other regulatory documents and research correspondence.
  • Supervise, mentor, and train new or junior research staff.
  • Coordinate with referring physicians to provide information regarding available research projects and maintain a strong referral basis.
  • Develop and maintain participant and study databases.
  • Coordinate protocols with collaborators at other institutions.
  • Assist the Principal Investigator and research team in the development of study protocols, study design, and preparation of research projects.
Minimum Qualifications

EQUIVALENCY STATEMENT: One year of higher education can be substituted for one year of directly related work experience (Example: bachelor's degree = 4 years of directly related work experience).

Job Levels:

  • Clinical Research Coordinator (Non-R.N.), I: Requires a bachelor's (or equivalency) + 2 years of directly related work experience or a master's (or equivalency) degree.
  • Clinical Research Coordinator (Non-R.N.), II: Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience.
  • Clinical Research Coordinator (Non-R.N.), III: Requires a bachelor's (or equivalency) + 6 years or a master's (or equivalency) + 4 years of directly related work experience.
Preferences
  • A BS in a relevant discipline, such as kinesiology, biomechanics, athletic training, physical therapy, engineering, or health science related field.
  • Exceptional organizational skills, attention to detail, and demonstrated human relations and effective communication skills.
  • Experience conducting human subject research and interacting with participants with impaired balance, mobility or neuromuscular control.
  • Experience working with and managing large participant databases such as REDCap.
  • Ability to excel in both team and individual environments.
  • Strong communication skills, both written and verbal.
  • Familiarity with biomechanical instrumentation including force plates, motion capture cameras, inertial measurement units, and electromyography.
Job Details
  • Seniority level:
    Associate
  • Employment type:

    Full Time
  • Job function:
    Research, Analyst, and Information Technology
  • Industry: Higher Education
  • Location:

    Campus
  • Pay Rate Range: $50,000–65,000 DOE
  • Requisition Number: PRN
    43842B
  • Close Date: 2/16/2026
  • Open Until Filled
Application

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