PS Regulatory Coordinator

University of Utah; Salt Lake City (UT); On-site; USD 39,300 - 61,384; Full time

Job summary

The Huntsman Cancer Institute (CTO) is hiring a coordinator to assist the Activation Project Administrator in various activation activities for oncology clinical trials conducted at Huntsman Cancer Institute.

Responsible for evaluating new clinical trial opportunities with faculty PIs and research managers, facilitating confidentiality agreements, feasibility, site visits, and tracking opportunities and outcomes.

Qualifications

• Bachelor's degree in a research or related area plus two years clinical trials/research experience or equivalency (one year of education can be substituted for two years of related work experience) required.
• One year of regulatory experience, an understanding of medical terminology and technical writing experience preferred.

Responsibilities

• Coordinates activation workflows to ensure appropriate timelines are met.
• Execution of confidentiality agreement for all clinical trial opportunities
• Assists in maintaining trial activation resources, brochures and start-up materials for activation process
• Completes feasibility questionnaires for clinical trials presented to the Clinical Trials Office
• Liaison with internal or external clients, sponsors, or partners for assigned studies, projects, or programs.
• Lead contact for all project matters; manage contractual and organizational client expectations; provide regular reports on status, metrics and issues.
• Manage project deliverables; track progress with metrics; follow-up on action items
• Represent the Clinical Trials Office in HCI Clinical Trial Research Group meetings
• Submit trial packages to Feasibility Administrative Review committee and follow-up on action items to achieve approval
• Liaise with the Office of Sponsored Projects and CTO Finance Pre-Award team to ensure CDA/CTA and study budgets are executed timely
• In cooperation with research managers, organize sponsor site visits
• Serve as internal liaison to bridge trials from activation to start-up
• Act as liaison between sponsors, investigators and CTO to evaluate problems and provide solutions
• Understand and act within regulatory frameworks and ethical guidelines for clinical research
• Promote a positive work environment through open communication
• Serve as first point of contact for outside CROs and sponsors
• Establish and foster relationships with investigators, sponsors and CTO staff
• Ensure high data quality and metrics to study sponsors and teams
• Assist in process and efficiency improvements in trial activation area
• Must be able to work independently with strong communication and human relations skills

Education

Bachelor's degree in a research or related area

Two years clinical trials/research experience

Job description

PS Regulatory Coordinator

Open Date: 10/20/2026

Requisition Number: PRN45615B

Job Title: PS Regulatory Coordinator

Working Title: Clinical Trial Activation Coordinator

Career Progression Track: E

Track Level:

FLSA Code: Administrative

Patient Sensitive Job Code?: Yes

Standard Hours per Week: 40

Full Time or Part Time?: Full Time

Shift: Day

Work Schedule Summary:

VP Area: President

Department: 01167 - HCI Clinical Trials Operations

Location: Campus

City: Salt Lake City, UT

Type of Recruitment: External Posting

Pay Rate Range: 39300 to 61384.25

Close Date: 10/20/2026

Job Summary

The Huntsman Cancer Institute (CTO) is hiring a coordinator to assist the Activation Project Administrator in various activation activities for oncology clinical trials conducted at Huntsman Cancer Institute. Responsible for assisting in evaluating new clinical trial opportunities for HCI with faculty principal investigators and clinical trial research managers and administrators. This will include assisting in facilitating and building strategic relationships with research partners; facilitation, tracking and execution of confidentiality agreements, completing feasibility questionnaires, conducting pre-study site visits, and tracking of the opportunities and outcomes. Serve as liaison with sponsors and vendors; assist with deliverables to clinical trial research multi-disciplinary teams; oversee project agreements; and nurture internal & external partnerships. Huntsman Cancer Institute is committed to cancer prevention, care, and survivorship for all communities within the area we serve - which includes Idaho, Montana, Nevada, Utah, and Wyoming - with impact worldwide. In your cover letter or during your interview process, we invite you to share how your professional experiences have prepared you to serve as a member of our team as we work to reduce the cancer burden experienced by all people and communities. This may include description of your prior experiences related to research, prevention, clinical care, community engagement/outreach, training, administration, or other areas relevant to Huntsman Cancer Institute's mission and this position.

Responsibilities

• 1. Coordinates activation workflows to ensure appropriate timelines are met.
• 2. Execution of confidentiality agreement for all clinical trial opportunities
• 3. Assists in maintaining trial activation resources, brochures and start-up materials for activation process
• 4. Completes feasibility questionnaires for clinical trials presented to the Clinical Trials Office
• 5. Liaison with internal or external clients, sponsors, or partners for assigned studies, projects, or programs. Lead contact for all project matters; understand and manage contractual and organizational client expectations; nurture client relationship and needs. Provide to the sponsor regular reports on project status, certain metrics, and issues.
• 6. Manage project deliverables. Track progress by keeping close metrics, including but not limited to time and quality. Be accountable for follow-up on action items. Work with the Project Administrator and Manager in identifying, resolving, or escalating issues.
• 7. Represent the Clinical Trials Office in HCI Clinical Trial Research Group meetings
• 8. Complete intake Clinical Trial Research Group new study review and prioritization forms.
• 9. Submit trial packages to the Feasibility Administrative Review committee and follow-up on action items to achieve approval.
• 10. Liaise with the Office of Sponsored Projects and CTO Finance Pre-Award team to ensure appropriate and timely execution of CDAs, CTAs and study budgets. Assist in scheduling calls and supporting negotiations in these areas.
• 11. In cooperation with research managers and administrators, organize and actively participate in sponsor site visits.
• 12. Serve as an internal liaison to bridge trials from activation to start-up.
• 13. Act as a liaison between study sponsors, HCI investigators and the Clinical Trials Office by evaluating problems and providing solutions.
• 14. Understand and act within the framework of regulatory guidelines provided by federal, state, and local regulatory agencies and ethical guidelines pertaining to the conduct of clinical research.
• 15. Promote a positive work environment that is maintained through open and effective communication.
• 16. Serve as first point of contact for potential outside CROs and sponsors. Be the face of the HCI CTO.
• 17. Establish and foster strong relationships and interactions with HCI investigators, study sponsors and the Clinical trials office personnel.
• 18. Ensure high quality of data and metrics to study sponsors and research teams.
• 19. Assist in process and efficiency improvements in the trial activation area.
• 20. Must be able to work independently and have strong communication and human relations skills.

Minimum Qualifications

Bachelor's degree in a research or related area plus two years clinical trials/research experience or equivalency (one year of education can be substituted for two years of related work experience) required; demonstrated human relations and effective communication skills also required. One year of regulatory experience, an understanding of medical terminology and technical writing experience preferred. This position is patient-sensitive and must fulfill all associated requirements. 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.

Preferences

• Bachelor's degree in a health sciences or related field with two years professional research experience in human subject research. Preferred Oncology Clinical Trials Experience. Exceptional organizational skills, attention to detail, and demonstrated human relations and effective communication skills also preferred.
• Knowledge of FDA regulations relevant to drugs, devices, biologics
• Previous working knowledge and experience with the pharmaceutical sponsors and contract research organizations
• Attention to detail with excellent analytical and problem-solving skills
• Thorough knowledge and understanding of medical, laboratory, and clinical trial concepts and terminology in oncology
• Ability to manage multiple tasks and set priorities and meet deadlines
• Work within a team approach and be motivated to work consistently in a fast-paced, "customer-focused" environment
• Excellent organizational and communication skills
• Skilled in Microsoft Office
• Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description.

Type

Benefited Staff

Additional Information

The University is a participating employer with Utah Retirement Systems ("URS"). Eligible new hires with prior URS service, may elect to enroll in URS if they make the election before they become eligible for retirement (usually the first day of work). Contact Human Resources at [phone] for information. Individuals who previously retired and are receiving monthly retirement benefits from URS are subject to URS’ post-retirement rules and restrictions. Please contact Utah Retirement Systems at [phone] or [phone] or University Human Resource Management at [phone] if you have questions regarding the post-retirement rules. This position may require the successful completion of a criminal background check and/or drug screen. The University of Utah values candidates who have experience working in settings with students and possess a strong commitment to improving access to higher education. Veterans' preference is extended to qualified applicants, upon request and consistent with University policy and Utah state law. Upon request, reasonable accommodations in the application process will be provided to individuals with disabilities. Consistent with state and federal law, the University of Utah does not discriminate based upon race, ethnicity, color, religion, national origin, age, disability, sex, sexual orientation, gender, gender identity, gender expression, pregnancy, pregnancy-related conditions, genetic information, or protected veteran's status. The University does not discriminate on the basis of sex in the education program or activity that it operates, as required by Title IX and 34 CFR part 106. The requirement not to discriminate in education programs or activities extends to admission and employment. Inquiries about the application of Title IX and its regulations may be referred to the Title IX Coordinator, to the Department of Education, Office for Civil Rights, or both. To request a reasonable accommodation for a disability or if you or someone you know has experienced discrimination or sexual misconduct including sexual harassment, you may contact the Director/Title IX Coordinator in the Office of Equal Opportunity and Title IX (OEO). More information, including the Director/Title IX Coordinator's office address, electronic mail address, and telephone number can be located at the University of Utah Non-Discrimination page. Online reports may be submitted at https://oeo.utah.edu. This report includes statistics about criminal offenses, hate crimes, arrests and referrals for disciplinary action, and Violence Against Women Act offenses. They also provide information about safety and security-related services offered by the University of Utah. A paper copy can be obtained by request at the Department of Public Safety located at 1658 East 500 South.

Posting Specific Questions

Required fields are indicated with an asterisk (*).

1. * Do you have a Bachelor's degree in a research or related area or equivalency? (2 years related work experience may be substituted for 1 year of education).
   • No
   • Yes
2. * How many years of clinical trials/research experience do you have?
   • Less than 2 years
   • 2 years or more, but less than 4 years
   • 4 years or more, but less than 6 years
   • 6 years or more, but less than 8 years
   • 8 years or more
3. Are you legally authorized to work in the United States?
   • Yes
   • No
4. Will you now or in the future require sponsorship for employment visa status (e.g., H-1B status)?
   • Yes
   • No
5. Do you have any current relatives working in HCI? (Open Ended Question)

Applicant Documents

Required Documents

1. Resume

Optional Documents

1. Cover Letter

University Human Resource Management 250 East 200 South, Suite 125 Salt Lake City, UT 84111 Contact us: [phone] By Email: [e-mail]