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PS Study Coordinator
University of Utah
- Salt Lake City, Utah, United States
- Salt Lake City, Utah, United States
About
Announcement
Details
Open Date 04/29/2026 Requisition Number PRN44882B Job Title PS Study Coordinator Working Title PS Study Coordinator Career Progression Track D 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 01233 - HCI INHERITED CANCER RES DEPT Location Campus City Salt Lake City, UT Type of Recruitment External Posting Pay Rate Range 31600 to 55000 Close Date 05/30/2026 Priority Review Date (Note - Posting may close at any time) Job Summary
Coordinates technical and administrative details involved in a clinical or research study. Assists the Principal Investigator in achieving study integrity and objectives through the successful implementation and completion of protocols and procedures.
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
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.
Essential Functions
* Assesses protocol for clarity and subject safety, reviews study inclusion/exclusion criteria; clarifies concerns and questions with Principal Investigator and sponsor.
* Attends and participates in Investigator and staff meetings. Advises team regarding specific study assignments and timelines.
* Explains and obtains informed consent, medical history and demographics; documents in source file and maintains with historical data, status reports, progress notes, and subject log to help ensure subject safety.
* Determines length of visits and coordinates related facility and equipment availability.
* Reports and tracks adverse events (AE). Reports serious AEs to IRB and sponsor.
* Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report for sponsor.
* Completes, audits, corrects CRFs, relays CRFs to sponsor.
* Assists with negotiating contract budget and
Languages
- English
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