Clinical Research Coordinator, III

Open Date: 06/01/2026 Requisition Number: PRN45226B Job Title: Clinical Research Coordinators (Non-R.N.) Working Title: Clinical Research Coordinator, III Career Progression Track: P00 Track Level: P3 - Career FLSA Code: Administrative Patient Sensitive Job Code? Yes Standard Hours per Week: 40 Full Time or Part Time? Full Time Shift: Day VP Area: U of U Health - Academics Department: 00868 - Psychiatry - Research Location: Campus City: Salt Lake City, UT Type of Recruitment: External Posting Pay Rate Range: $57,000 Close Date: 07/01/2026 Job Summary This clinical research coordinator position will involve assisting with a NIDA‑funded UG3/UH3 trial of ketamine‑assisted psychotherapy for patients with opioid use disorder on buprenorphine. The study compares an 8‑week Mindfulness‑Oriented Recovery Enhancement (MORE) + 2 ketamine sessions to an 8‑week supportive therapy intervention + 2 ketamine sessions. In addition to clinical outcomes and experiential outcomes, we are tracking with this trial, we will be examining dyadic EEG synchrony between study participants and the study therapist to better understand how therapeutic alliance, connection, and engagement predict therapeutic outcomes in psychedelic‑assisted therapies. This role will involve coordination of day‑to‑day clinical trial activities in accordance with Good Clinical Practices (GCPs), study protocols, and applicable regulations, implementation processes, and organization of efforts within the study team to achieve objectives, and coordination of research procedures, study visits, and follow‑up care. This role will also involve maintaining tools and documentation to track study outcomes and providing updates to regulatory bodies and the study team, maintaining source documents, assessing and reporting adverse events (AEs), recruiting, screening, and obtaining consent from study participants, as well as interacting directly with study participants and their families/interpersonal supports. This role will work alongside another full‑time clinical research coordinator and a team of study therapists, co‑investigators, and the PI, Benjamin Lewis, MD. Responsibilities Coordinate and manage day‑to‑day clinical trial operations in compliance with Good Clinical Practice guidelines, study protocols, institutional policies, and applicable local, state, and federal regulations. Independently plan, organize, and implement complex study activities to meet protocol objectives, including scheduling and conducting study visits, procedures, and required follow‑up. Serve as an operational liaison along with another full‑time coordinator for assigned studies, collaborating effectively with Principal Investigators, study sponsors, clinical teams, ancillary departments, external partners, and regulatory entities. Lead participant recruitment, screening, enrollment, and informed consent processes, ensuring ethical conduct, protocol adherence, and subject safety. Collect, review, and maintain accurate and complete source documentation, regulatory binders, and study records, ensuring audit and inspection readiness at all times. Coordinate and support pre‑study feasibility, site qualification, study initiation, monitoring, and close‑out visits, including preparation of materials and timely resolution of action items. Identify, document, and report adverse events, serious adverse events, and protocol deviations in accordance with regulatory requirements and sponsor timelines. Oversee collection, entry, and quality control of participant, clinical, and laboratory data, resolving queries and discrepancies with minimal oversight. Develop, maintain, and utilize tracking tools to monitor study milestones, enrollment progress, regulatory deadlines, and other key performance metrics, providing regular updates to investigators and management. Apply advanced knowledge and independent judgment to troubleshoot complex study issues, elevate risks appropriately, and recommend process improvements. Provide guidance, training, or informal mentorship to junior research staff, contributing to team effectiveness and consistent application of best practices. Maintain participant‑focused communication, working directly with research participants and families to support engagement, education, and retention throughout the study lifecycle. 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). Clinical Research Coordinator (Non‑R.N.), III : Requires a bachelor’s (or equivalency) + 6 years or a master’s (or equivalency) + 4 years of directly related work experience. Preferences 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 View phone number on click.appcast.io 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 View phone number on click.appcast.io or View phone number on click.appcast.io or University Human Resource Management at View phone number on click.appcast.io 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. 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. 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