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

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://utah.peopleadmin.com/postings/208758

Posted by the FREE value-added recruitment advertising agency

je-037a560f875a48c6bf96e6678fb705ad

CRSF Program Training Specialist

Job Description

Looking for more opportunities?