Job Details

University of Utah
  • Position Number: 7209348
  • Location: Salt Lake City, UT
  • Position Type: Assessment, Accreditation, and Compliance


Regulatory Specialist

Job Summary

Job Summary:
The Division of Neurology in the Department of Pediatrics is seeking a Regulatory Affairs Specialist to support clinical research activities at the University of Utah Spencer F. Eccles School of Medicine. This position is responsible for preparing, submitting, and tracking regulatory documents to ensure compliance with institutional, federal, and sponsor requirements. The Regulatory Affairs Specialist will collaborate with study teams, institutional review boards (IRB), and external sponsors to support study start-up, maintenance, and closeout activities.

The role involves maintaining regulatory documentation, supporting audits and inspections, and ensuring adherence to applicable regulations and guidelines. The incumbent will also assist in monitoring regulatory changes and communicating updates to study teams to support ongoing compliance.

This position is posted at multiple job levels. Each level has distinct qualifications, responsibilities, which will be evaluated during the selection process. Final placement, including the associated pay rate, will be determined based on business needs and budget considerations.

Department Summary:
The Department of Pediatrics is the second largest department in the University of Utah School of Medicine and one of the largest pediatric departments in the country. We are committed to improving the lives of children through excellence in advocacy, education, research, and clinical care. For more information about the Department of Pediatrics, please visit: http://medicine.utah.edu/pediatrics/. Mutual respect and appreciation are highly valued in the department.
Benefits Summary:
The University of Utah offers a comprehensive benefits package including:
Additional benefits information is available at https://benefits.utah.edu/.


Employee Health Requirements:
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. We protect our patients, coworkers and community by requiring all patient-sensitive employees to be immunized according to CDC standards and hospital policy. Limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations.

Responsibilities
Essential Functions:Prepare, submit, and track regulatory documents and submissions. Ensure submissions are complete, timely, and regulatory objectives are met. Research scientific and regulatory information in order to write, edit, and review reports. Work with various governmental and regulatory bodies (e.g., FDA, MHRA, EMA) to ensure compliance and expedite approval of pending registration. Compile all material required for submissions, license renewals, and annual registrations. Identify relevant guidance documents and interpret international/consensus standards. Participate in internal or external audits and inspections.

1. Prepare and submit IRB applications, amendments, and reports to support study start-up and ongoing compliance.2. Track IRB submissions, complete required revisions, and ensure adherence to established timelines.3. Prepare and maintain study training logs and regulatory documentation (e.g., DOA logs).4. Manage and maintain regulatory binders/ISF and associated study documentation.5. Ensure all regulatory documents, certifications, and licenses are current and maintained.6. Monitor updates to University of Utah IRB policies and processes and apply changes to study activities.7. Communicate regulatory and IRB updates to study teams to ensure ongoing compliance.8. Review and maintain familiarity with active study protocols to support regulatory requirements.9. Collaborate with study teams and sponsors to finalize regulatory documents (e.g., ICFs).10. Ensure timely completion of regulatory submissions and revisions in accordance with study timelines.11. Assist in the development and maintenance of internal SOPs, as needed.12. Assist with additional regulatory or study-related tasks as needed to support compliance and operational objectives.

The following job levels and associated pay rates will be considered based on job placement. Final placement, including the corresponding pay rate, will be determined by the department in alignment with business needs and budget considerations.
Regulatory Affairs Specialist (Life Sciences), I
Requires basic skill set and proficiency. Conducts work assignments as directed. Closely supervised with little latitude for independent judgment.
Requires a bachelor's (or equivalency) with up to 2 years of directly related work experience or a master's (or equivalency) degree.This is an Entry-Level position in the General Professional track.Job Code: PZ6891Grade: P13Expected Pay Range: $46,584 to $57,976

Regulatory Affairs Specialist (Life Sciences), IIRequires moderate skill set and proficiency in discipline. Conducts work assignments of increasing complexity, under moderate supervision with some latitude for independent judgment.
Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience.This is a Developing-Level position in the General Professional track.Job Code: PZ6892Grade: P14Expected Pay Range: $51,242 to $69,629

Regulatory Affairs Specialist (Life Sciences), IIIConsidered highly skilled and proficient in discipline. Conducts complex, important work under minimal supervision and with wide latitude for independent judgment.
Requires a bachelor's (or equivalency) + 6 years or a master's (or equivalency) + 4 years of directly related work experience.This is a Career-Level position in the General Professional track.Job Code: PZ6893Grade: P16Expected Pay Range: $62,004 to $84,252

Regulatory Affairs Specialist (Life Sciences), IVRecognized as subject matter expert and advanced individual contributor professional. Requires specialized skill set. Conducts highly complex work, unsupervised and with extensive latitude for independent judgment.
Requires a bachelor's (or equivalency) + 8 years or a master's (or equivalency) + 6 years of directly related work experience.This is an Advanced-Level position in the General Professional track.Job Code: PZ6894Grade: P17Expected Pay Range: $68,204 to $92,678
Disclaimer:This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.


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:
Regulatory Affairs Specialist (Life Sciences), I: Requires a bachelor's (or equivalency) + 2 years of directly related work experience or a master's (or equivalency) degree. Regulatory Affairs Specialist (Life Sciences), II: Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience. Regulatory Affairs Specialist (Life Sciences), III: Requires a bachelor's (or equivalency) + 6 years or a master's (or equivalency) + 4 years of directly related work experience. Regulatory Affairs Specialist (Life Sciences), IV: Requires a bachelor's (or equivalency) + 8 years or a master's (or equivalency) + 6 years of directly related work experience.


Preferences
Preferences:
  • Experience with University of Utah IRB.
  • Clinical research regulatory experience.
  • CITI Training (or to be completed within 1 month of hire).



The Department will screen applicants according to the identified preferences.

Special Instructions


Requisition Number: PRN45245B
Full Time or Part Time? Full Time
Work Schedule Summary: Monday - Friday, 8:00 a.m. - 5:00 p.m. Hours may vary based on operational needs. Opportunities for a hybrid telework schedule may be considered after the initial training period, provided the arrangement is supported by operational needs and individual performance. Telework arrangements are not guaranteed and may be modified or discontinued at any time based on business requirements or performance. Employees approved for hybrid telework must provide their own private workspace, secure internet connection, and demonstrate the ability to work independently.
Department: 00848 - Pediatric Administration
Location: Campus
Pay Rate Range: Depends on Experience
Close Date: 9/3/2026
Open Until Filled:

To apply, visit https://utah.peopleadmin.com/postings/203047







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