PS Clinical Research Coord

Details

Open Date 01/14/2026

Requisition Number PRN
44026B

Job Title PS Clinical Research Coord

Working Title PS Clinical Research Coord

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 U of U Health - Academics

Department 00952 - Division of Epidemiology

Location Campus

City Salt Lake City, UT

Type of Recruitment External Posting

Pay Rate Range 39300 to 72700

Close Date 03/13/2026

Priority Review Date (Note - Posting may close at any time)

This position is within the Division of Epidemiology’s Program for Addiction Research, Clinical Care, Knowledge, and Advocacy (PARCKA)
(Use the "Apply for this Job" box below)./parcka
. This position will coordinate the implementation, quality control and completion of research studies while assisting the Principal Investigator in determining and accomplishing study objectives. Oversees research studies in an administrative and operational capacity while maintaining compliance with guidelines set by governing agencies. PARCKA’s studies are conducted at various clinics in the Salt Lake City area. Job duties will require interaction with study participants, investigators, clinic and research staff, and study monitors.

The incumbent will work closely with the project team to achieve study integrity and objectives through the successful implementation and completion of protocols and procedures.

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.

• Oversees compliance to protocol; manages quality control, completion and submission of study related documentation; prepares reports for organizations and agencies.
• 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.
• Recognizes, tracks and reports adverse events and protocol deviations and other events as outlined in the protocol.
• Helps prepare and coordinate site visits made by sponsors or federal agencies during course and at the close of the study.
• May represents the research program at meetings, national and international research consortia.
• May prepare, submit and maintain IRB , FDA , NCI , NIH , NSF and/or other regulatory documents and research correspondence.
• Contributes to developing educational materials and educates the community and other research professionals regarding studies and related research issues.
• May supervise, mentor and train new or junior research staff.
• Coordinates with referring physicians to provide information regarding available research projects and to maintain a strong referral basis.
• May develop and maintain patient databases, investigational logs and records of drugs administered, medical devices monitored and/or procedures followed.
• May assists the Principal Investigator in the development of study protocols.

Four years of Research experience is preferred, along with Microsoft and Excel knowledge.

The incumbent decides how to best accomplish the daily requirements of various study objectives, prioritizes and delegates workload and establishes systems needed to achieve specific study goals. Efforts of multiple departments or disciplines must be coordinated to ensure effective follow through and compliance of all involved. The incumbent functions independently under minimal supervision, following FDA , Good Clinical Practice, IRB , NIH , NCI , NSF and/or other regulatory agency guidelines and seeking…