CRSF Program Training Specialist
Job Summary
CRSF Program Training Specialist
The Clinical and Translational Science Institute is seeking a
highly motivated individual to join our Clinical Research Support
Office (CRSO) as a CRSF Program Training Specialist. The CRSF
Program Training Specialist is responsible for the design,
development, and delivery of training programs and educational
content to support clinical research coordinators and study teams.
This role focuses on teaching and creating structured,
competency-based learning materials that promote high-quality,
compliant, and efficient clinical research practices across the
institution. This program specialist collaborates with
institutional stakeholders to ensure training programs align with
federal regulations, Good Clinical Practice (GCP), and University
policies, with an emphasis on human subject's research protections
and regulatory compliance.
Responsibilities
CRSF Program Training Specialist Responsibilities
- Develop, design, and implement training materials, tools, and
targeted curriculum for clinical research coordinators and study
teams
Create role-based and competency-driven training content that
supports the safe and compliant conduct of clinical research
Ensure all materials align with human subject's research
protections, GCP, FDA regulations, and institutional policies
Organize, maintain, and regularly update training materials to
reflect evolving regulatory requirements and best practices
Support development and delivery of clinical research training
programs, including continuing education for coordinators
Assist in standardizing training approaches across departments
to ensure consistency and quality
Participate in the evaluation and continuous improvement of
training programs using feedback and performance metrics
Coordinate training content development with departments across
campus and external stakeholders
Partner with CRSO teams, IRB, and compliance offices to ensure
training reflects real-world research processes and institutional
expectations
Establish and maintain collaborative relationships to support
ongoing training initiatives and workforce development efforts
Other duties as assigned
Requires a bachelor's (or equivalency) + 6 years or a master's (or
equivalency) + 4 years of directly related work experience.
Minimum Qualifications
EQUIVALENCY STATEMENT: 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).
Department may hire employee at one of the following job
levels:
Program Specialists, III: Requires a bachelor's
(or equivalency) + 6 years or a master's (or equivalency) + 4 years
of directly related work experience.
Preferences
Preferences:
- Experience working in an academic medical center or clinical
research environment
- Familiarity with:
- Good Clinical Practice (GCP)
- FDA regulations and IRB processes
Experience supporting or delivering training for clinical
research coordinators or study teams
Special Instructions
In the cover letter, please describe your experience as it relates
to this position and confirm that you will be available to work
from the state of Utah for this position.
Requisition Number: PRN46105B
Full Time or Part Time? Full Time
Work Schedule Summary: Business hours, arranged with
supervisor
Department: 02148 - Clinical Research Service Ofc
Location: Campus
Pay Rate Range: $63,000-$70,000
Close Date: 12/02/2026
Open Until Filled:
To apply, visit https://apptrkr.com/9802711"">https://utah.peopleadmin.com/postings/208758
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