What are the responsibilities and job description for the Clinical Research Coordinator - II position at Pantheon Clinical Research?
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 inspections
- Maintain 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 with minimal supervision
- Ability to prioritize and manage multiple ongoing studies
Preferred Qualifications
- Bachelor's or Associate's degree in a health-related or life sciences field
- CCRC or CCRP certification
- Experience with RealTime, Medrio, Rave, Florence, or similar research systems
- Experience in Internal Medicine, Endocrinology, Dermatology, Pulmonology, CNS, or Vaccine studies
- Phlebotomy experience
Compensation
$28.37 - $31.25 per hour DOE
(Approximately $59,000 - $65,000 annually based on a 40-hour workweek)
Compensation is based on experience, qualifications, and demonstrated clinical research expertise.
Benefits
- Paid time off
- Paid holidays
- SIMPLE IRA with company matching contribution
- Employer-paid research training and professional development courses
- Opportunities for advancement within a growing organization
- Pantheon does not currently offer medical benefits
Why Join Pantheon?
Pantheon Clinical Research is a growing independent research site dedicated to advancing medicine through high-quality clinical trials and exceptional patient care.
Unlike many large corporate research organizations, Pantheon offers a collaborative environment where team members have a direct impact on study success, patient experience, and operational improvement. Our team works closely together, decisions are made efficiently, and new ideas are welcomed. Employees have the opportunity to take ownership of their work, develop meaningful relationships with patients and sponsors, and contribute directly to the growth and success of the organization.
We value professionalism, accountability, continuous learning, and a commitment to excellence. If you are looking for a place where your contributions are recognized and your work truly makes a difference, we'd love to hear from you.
Pay: $59,000.00 - $65,000.00 per year
Benefits:
- Paid time off
Application Question(s):
- Do you currently reside in Davis, Weber, Salt Lake, or Utah County?
- Have you independently managed industry-sponsored clinical trials?
- Have you independently conducted informed consent visits?
- Which EDC systems have you used?
- What is your desired hourly rate?
Experience:
- Clinical Research Coordinator: 2 years (Preferred)
Ability to Commute:
- Bountiful, UT 84010 (Preferred)
Work Location: In person
Salary : $59,000 - $65,000