University of Utah ยท 1 day ago
Clinical Research Coordinator
Salt Lake City, UT
Full-time
Onsite
Mid, Senior Level
$58K/yr - $70K/yr
4+ years expUniversity of Utah is seeking a Clinical Research Coordinator to oversee day-to-day clinical trial activities in adherence to Good Clinical Practices and study protocols. The role involves coordinating research procedures, maintaining documentation, and working closely with study participants and other departments.
Higher Education
Responsibilities
Oversees compliance to protocol; manages quality control, completion and submission of study-related documentation; prepares reports for organizations and agencies
Monitors enrollment goals and initiates strategies to promote enrollment and participant compliance. Coordinates and performs 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, overseeing study visits, and acting as a liaison between participants and study-related parties
Recognizes, tracks, and reports adverse events and protocol deviations
Prepares for and coordinates site visits made by sponsors during course and at the close of the study
Prepares, submits, and maintains IRB and/or other regulatory documents and research correspondence
Contributes to developing educational materials and educates the community and other research professionals regarding studies and related research issues
Coordinates with treating providers and staff to provide information regarding research projects and to maintain a strong relationship
Qualification
Required
Must fulfill all associated vaccination requirements, or be approved for an exemption, prior to the first day of work
Coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices (GCPs), study protocols, and applicable regulations
Implement processes and organize efforts within study team to achieve objectives, coordinating research procedures, study visits, and follow-up care
Create and maintain tools and documentation to track study metrics, providing updates to management
Conduct pre-study, site qualification, study initiation, monitoring visits, and close-out activities
Maintain source documents and report adverse events
Recruit, screen, enroll, and obtain consent from study participants
Collect and maintain patient and laboratory data
Work directly with study participants and families and serve as project liaison to other departments, outside organizations, and government agencies
Work under the direction of the Primary Investigator (PI) and division manager
Oversees compliance to protocol; manages quality control, completion and submission of study-related documentation; prepares reports for organizations and agencies
Monitors enrollment goals and initiates strategies to promote enrollment and participant compliance
Coordinates and performs 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, overseeing study visits, and acting as a liaison between participants and study-related parties
Recognizes, tracks, and reports adverse events and protocol deviations
Prepares for and coordinates site visits made by sponsors during course and at the close of the study
Prepares, submits, and maintains IRB and/or other regulatory documents and research correspondence
Contributes to developing educational materials and educates the community and other research professionals regarding studies and related research issues
Coordinates with treating providers and staff to provide information regarding research projects and to maintain a strong relationship
1 year of higher education can be substituted for 1 year of directly related work experience
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
Company
University of Utah
The University of Utah, located in Salt Lake City in the foothills of the Wasatch Mountains, is the flagship institution of higher learning in Utah.
10001+ employees
H1B Sponsorship
University of Utah has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (216)
2024 (189)
2023 (201)
2022 (175)
2021 (156)
2020 (174)
Funding
Current Stage
Late StageLeadership Team
Allison Nicholson
Special Assistant to CFO
Bruce Hunter
Interim Chief Innovation and Economic Engagement Officer
Recent News
National Institutes of Health (NIH)
2023-06-27
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