Clinical Research Coordinator

Overview Pantheon Clinical Research is seeking an experienced Clinical Research Coordinator to manage active industry-sponsored clinical trials. This is a full-time, on-site position based in Bountiful, Utah. Applicants must currently reside in Davis, Weber, Salt Lake, or Utah County and be able to reliably commute to our office. Relocation assistance is not available. Applications from outside the local commuting area will not be considered. The ideal candidate will have at least two years of clinical research coordination experience and be capable of independently managing study activities, participant visits, sponsor interactions, and data collection while maintaining the highest standards of regulatory compliance and patient care. Responsibilities Coordinate day-to-day operations of assigned clinical trialsScreen, consent, enroll, and schedule study participantsConduct study visits and protocol-required proceduresEnsure compliance with ICH-GCP, FDA regulations, IRB requirements, and sponsor protocolsMaintain accurate source documentationEnter study data into EDC systems and resolve data queriesCoordinate laboratory collections, processing, and shipmentsTrack investigational product, study supplies, and laboratory kitsCommunicate effectively with sponsors, CROs, monitors, investigators, and participantsPrepare for monitoring visits, audits, and inspectionsMaintain essential regulatory and study documentationManage multiple studies simultaneously while meeting enrollment and data-quality goals Required Qualifications Minimum 2 years of Clinical Research Coordinator experienceExperience managing industry-sponsored clinical trialsWorking knowledge of ICH-GCP, FDA, and IRB regulationsExperience with EDC and CTMS platformsStrong organizational and time-management skillsExcellent written and verbal communication skillsAbility to work independently and manage multiple active clinical trials Preferred Qualifications Bachelor's degree in a health sciences, life sciences, or related fieldCCRC, CCRP, or similar clinical research certificationExperience with systems such as RealTime CTMS, Rave, Medrio, or comparable clinical trial platforms The degree, certification, and named-platform preferences were part of the earlier posting you supplied and asked me to blend into the revised version. Compensation $28.37–$31.25 per hour, depending on experience and qualifications. This corresponds to approximately $59,000–$65,000 annually for a full-time position. The $59,000–$65,000 range was the compensation level you specifically selected in the final revision. Benefits & Professional Development SIMPLE IRA retirement plan with company matchPaid clinical research training and professional-development coursesOpportunities to expand clinical research knowledge and responsibilities We specifically removed health insurance and 401(k) language because you said Pantheon did not offer those benefits. You also clarified that Pantheon pays for applicable training courses rather than offering certification reimbursement. Why Join Pantheon? Pantheon Clinical Research offers an environment that is different from what employees may experience at large, corporate-run research organizations. As an independent research site, we offer the opportunity to work closely with investigators, leadership, sponsors, and fellow research professionals in a collaborative setting where individual contributions have a visible impact. Our coordinators are not simply assigned to one narrow piece of the clinical trial process. They have the opportunity to develop broad experience across study operations, participant care, sponsor interactions, data quality, and regulatory compliance. We value professionalism, accountability, attention to detail, and a genuine commitment to providing an excellent experience for both study participants and our research partners. Powered by JazzHR X3D7lQV4bR