Clinical Research Coordinator

Pantheon Clinical Research; Bountiful (UT); On-site; USD 59,000 - 65,000; Full time

Benefits offered by this job

SIMPLE IRA with company match

Paid clinical research training

Professional development opportunities

Job summary

Pantheon Clinical Research in Bountiful, Utah is seeking an experienced Clinical Research Coordinator to manage active industry-sponsored trials on a full-time, on-site basis.

The candidate should have at least two years of coordinator experience, be able to independently manage study visits, sponsor interactions, and data collection while maintaining regulatory compliance.

Compensation ranges from $28.37 to $31.25 per hour, approximately $59k–$65k annually for full-time.

Qualifications

• 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.

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 inspectionsMaintain essential regulatory and study documentation
• Manage multiple studies simultaneously while meeting enrollment and data-quality goals

Skills

Clinical Research Coordination

Regulatory compliance

Documentation & data entry

Communication skills

Independent work

Education

Bachelor's degree in health sciences or related field

Tools

RealTime CTMS

Rave

Medrio

EDC platforms

CTMS systems

Job description

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 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 inspectionsMaintain essential regulatory and study documentation
• Manage multiple studies simultaneously while meeting enrollment and data-quality goals

Required Qualifications

• 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

Preferred Qualifications

• Bachelor's degree in a health sciences, life sciences, or related field
• CCRC, 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 match
  • Paid clinical research training and professional-development courses
  • Opportunities 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.