University of Utah Health Research · 4 hours ago
Clinical Research Coordinator
University of Utah Health Research is looking for a Clinical Research Coordinator to manage day-to-day clinical trial activities. The role involves coordinating research procedures, study visits, and follow-up care while ensuring compliance with Good Clinical Practices and study protocols.
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
1 year of higher education can be substituted for 1 year of directly related work experience (Example: bachelor's degree = 4 years 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
Must fulfill all associated vaccination requirements, or be approved for an exemption, prior to the first day of work
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
Coordinates with treating providers and staff to provide information regarding research projects and to maintain a strong relationship
Experience working in settings with students and possess a strong commitment to improving access to higher education
This position may require the successful completion of a criminal background check and/or drug screen
Benefits
The University is a participating employer with Utah Retirement Systems (“URS”). Eligible new hires with prior URS service, may elect to enroll in URS if they make the election before they become eligible for retirement (usually the first day of work).
Company
University of Utah Health Research
At University of Utah Health, our world-class researchers work together to tackle some of the toughest problems in health and medicine.
Funding
Current Stage
Late StageCompany data provided by crunchbase