Clinical Research Coordinator

Pantheon Clinical Research is seeking a Clinical Research Coordinator to manage active industry-sponsored clinical trials. The role oversees study operations, participant visits, sponsor interactions, data collection, and regulatory compliance while supporting high-quality patient care.

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 effectively 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

Preferred

Bachelor's degree in a health sciences, life sciences, or related field

CCRC, CCRP, or similar clinical research certification

Experience with systems such as RealTime CTMS, Rave, Medrio, or comparable clinical trial platforms

Bachelor's degree

Health sciences

Life sciences

CCRC certification

CCRP certification

Clinical research certification

RealTime CTMS

Rave

Medrio

Clinical trial platforms

Benefits

SIMPLE IRA retirement plan with company match

Paid clinical research training and professional-development courses

Opportunities to expand clinical research knowledge and responsibilities

Company

Pantheon Clinical Research conducts clinical trials and neurology and metabolic studies for patients, sponsors, and physicians.

Bountiful, Utah, USA

https://www.pantheonclinical.com/

Founded in 2022

2-10 employees

Qualifications

Applicants must currently reside in Davis, Weber, Salt Lake, or Utah County

Minimum 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

Bachelor's degree in a health sciences, life sciences, or related field

CCRC, CCRP, or similar clinical research certification

Experience with systems such as RealTime CTMS, Rave, Medrio, or comparable clinical trial platforms

Required skills

Clinical Research Coordination, Industry-Sponsored Clinical Trials, ICH-GCP, FDA Regulations, IRB Regulations, Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), CCRC, CCRP, RealTime CTMS, Rave, Medrio

Preferred skills

CCRC, CCRP, or similar clinical research certification

Experience

2+ years