Clinical Research Coordinator

Pantheon Clinical Research•Bountiful, UT

22d•Onsite

About The Position

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 the office. Relocation assistance is not available, and applications from outside the local commuting area will not be considered. The ideal candidate has at least two years of clinical research coordination experience and can independently manage study activities, participant visits, sponsor interactions, and data collection while maintaining regulatory compliance and patient care standards. As an independent research site, Pantheon offers the opportunity to work closely with investigators, leadership, sponsors, and fellow research professionals in a collaborative environment. Coordinators can develop broad experience across study operations, participant care, sponsor interactions, data quality, and regulatory compliance. The company values professionalism, accountability, attention to detail, and a commitment to a positive experience for study participants and research partners.

Requirements

At least 2 years of Clinical Research Coordinator experience.
Experience managing industry-sponsored clinical trials.
Working knowledge of ICH-GCP, FDA, and IRB regulations.
Experience with EDC and CTMS platforms.
Strong organizational and time-management skills.
Excellent written and verbal communication skills.
Ability to work independently and manage multiple active clinical trials.
Currently reside in Davis, Weber, Salt Lake, or Utah County and be able to reliably commute to the Bountiful office.

Nice To Haves

Bachelor's degree in a health sciences, life sciences, or related field.
CCRC, CCRP, or similar clinical research certification.
Experience with RealTime CTMS, Rave, Medrio, or comparable clinical trial platforms.

Responsibilities

Coordinate day-to-day operations of assigned clinical trials.
Screen, consent, enroll, and schedule study participants.
Conduct study visits and protocol-required procedures.
Ensure compliance with ICH-GCP, FDA regulations, IRB requirements, and sponsor protocols.
Maintain accurate source documentation.
Enter study data into EDC systems and resolve data queries.
Coordinate laboratory collections, processing, and shipments.
Track investigational product, study supplies, and laboratory kits.
Communicate with sponsors, CROs, monitors, investigators, and participants.
Prepare for monitoring visits, audits, and inspections.
Maintain essential regulatory and study documentation.
Manage multiple studies simultaneously while meeting enrollment and data-quality goals.