Clinical Research Coordinators (Non-R.N.)

Requisition Number: PRN45727B

Location: Salt Lake City, UT | Full-time, 40 hours per week, day shift | On-site

About the Role

Clinical Research Coordinators (Non-R.N.) coordinate day-to-day clinical trial activities in adherence to Good Clinical Practices (GCPs), study protocols, and applicable regulations. This position is within the Division of Epidemiology’s Program for Addiction Research, Clinical Care, Knowledge, and Advocacy (PARCKA). PARCKA’s studies are conducted at various clinics in the Salt Lake City area. Job duties are 100% on-site and require interaction with study participants, investigators, clinic and research staff, and study monitors.

Responsibilities

• Implement processes and organize efforts within the 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).

Requirements

The department may hire at one of the following levels based on business need and budget:

• Clinical Research Coordinator (Non-R.N.), II (Developing-Level):
  • Bachelor’s degree (or equivalency) + 4 years of directly related work experience, or
  • Master’s degree (or equivalency) + 2 years of directly related work experience.
  • Conducts work assignments of increasing complexity under moderate supervision with some latitude for independent judgment.
• Clinical Research Coordinator (Non-R.N.), III (Career-Level):
  • Bachelor’s degree (or equivalency) + 6 years of directly related work experience, or
  • Master’s degree (or equivalency) + 4 years of directly related work experience.
  • Considered highly skilled and proficient in discipline; conducts complex, important work under minimal supervision with wide latitude for independent judgment.
• Clinical Research Coordinator (Non-R.N.), IV (Advanced-Level):
  • Bachelor’s degree (or equivalency) + 8 years of directly related work experience, or
  • Master’s degree (or equivalency) + 6 years of directly related work experience.
  • Recognized as a subject matter expert and advanced individual contributor; conducts highly complex work unsupervised with extensive latitude for independent judgment.

Equivalency Statement: 1 year of higher education can substitute for 1 year of directly related work experience (e.g., bachelor’s degree = 4 years of experience).

Pay

• Clinical Research Coordinator (Non-R.N.), II: $29,913 to $68,625
• Clinical Research Coordinator (Non-R.N.), III: $36,196 to $83,036
• Clinical Research Coordinator (Non-R.N.), IV: $39,815 to $91,340
• Overall Pay Range: $36,000 to $70,000

Benefits

The University of Utah offers a comprehensive benefits package. Learn more at benefits.utah.edu.

• Eligible new hires with prior Utah Retirement Systems (URS) service may enroll in URS before becoming eligible for retirement.
• Post-retirement rules apply to individuals receiving monthly retirement benefits from URS.
• This position may require a criminal background check and/or drug screen.