PS Clinical Research Coord

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45594B Job Title PS Clinical Research Coord Working Title Clinical Research 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 02059 - HCI Popul Sci Trials Office Location Campus City Salt Lake City, UT Type of Recruitment External Posting Pay Rate Range 39300 to 60000 Close Date 10/20/2026 Priority Review Date (Note - Posting may close at any time)

Job Summary

The Population Sciences Research Infrastructure, Systems, and Management team has an immediate opening for a Clinical Research Coordinator within the Population Sciences Trials Office and Adapt team at Huntsman Cancer Institute. This role partners with Principal Investigators to support high-quality, ethical, and compliant research aimed at improving cancer outcomes and prevention, while overseeing study operations and regulatory requirements across investigator-initiated and sponsored projects.

The position will specifically support the Hematologic Malignancies (Heme) Adapt program, contributing to research within a specialized disease center focused on hematologic cancers.

The Population Sciences Trials Office (PSTO)/Adapt supports Investigators conducting observational and behavioral intervention studies aimed at preventing cancer in different populations and/or at improving outcomes and the quality of life among those diagnosed with cancer. This coordinator will work with a collaborative team of study support staff under the direction of the PSTO/Adapt research manager to support the Principal Investigator's research objectives.

Depending on study needs, employees may have a hybrid work schedule after completing a probationary period, working both remotely as well as on-site. Employees may need to provide their own home office space, internet connection, telephone, and can work independently.

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. Partnerships with individuals, communities, and many other entities are crucial to our work. Huntsman Cancer Institute values cancer-related health equity and inclusion as integral to our guiding principle to serve our patients and their communities, and our commitment to foster a culture of belonging for all within our organization.

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

This position will coordinate the technical and administrative details involved in a clinical or research study, including but not limited to, the following:

* Providing back-up team coverage when needed.

* Support various projects related to this specific cancer type,

* Attend meetings and consult with the Hematology (Heme) Disease Center, and other research teams.

Responsible for study maintenance.

Uphold institutional and departmental expectations and policies.

Anticipate potential challenges and proactively seek solutions to avoid or mitigate existing and future problems.

Study Operations

* Assists in study-specific training for junior staff members

* Oversees compliance to protocol; manages quality control, completion and submission of study related documentation; assist in preparation of reports for organizations and agencies.

* Oversee, assess and ensure participant safety and strict protocol implementation/adherence.

* Monitors enrollment goals and initiates strategies to promote enrollment and participant compliance.

* Coordinates and performs responsibilities related to research participants including determining subject population availability, developing informed consents and screening materials, screening and recruiting subjects, scheduling visits, obtaining informed consent, answering subject inquiries, overseeing study visits and acting as a liaison between participants and study-related parties.

* Represents the research program at meetings, national and international research consortia.

* Prepare for and coordinate site visits made by sponsors or federal agencies during course and at the close of the study.

* Contributes to developing educational materials and educates the community and other research professionals regarding studies and related research issues.

* Coordinates with referring physicians to provide information regarding available…