University of Utah Health Research · 13 hours ago
Clinical Research Coordinators (Non-R.N.)
Salt Lake City, UT
Full-time
Onsite
Entry, Mid, Senior Level
$35K/yr - $50K/yr
2+ years expUniversity of Utah Health Research is seeking Clinical Research Coordinators (Non-R.N.) to coordinate day-to-day clinical trial activities. The role involves adherence to Good Clinical Practices (GCPs), managing study protocols, and providing updates to management while working closely with study participants and families.
Higher Education
Responsibilities
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)
Qualification
Required
Requires a bachelor's (or equivalency) + 2 years of directly related work experience or a master's (or equivalency) degree
Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience
Requires a bachelor's (or equivalency) + 6 years or a master's (or equivalency) + 4 years of directly related work experience
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
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)
Preferred
The University of Utah values candidates who have experience working in settings with students from all backgrounds and possess a strong commitment to improving access to higher education for historically underrepresented students
Individuals from historically underrepresented groups, such as minorities, women, qualified persons with disabilities and protected veterans are encouraged to apply
Veterans' preference is extended to qualified applicants, upon request and consistent with University policy and Utah state law
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.
5001-10000 employees
Funding
Current Stage
Late StageCompany data provided by crunchbase