Clinical Research Coordinator (Clinical Research)

Location: Fully on-site in Bountiful, Utah, United States

Salary: $36,600–$91,300 annual base pay

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The role is based within Avacare, a site management organization backed by IQVIA’s global CRO resources.

What you will do

• Coordinate 2–6 clinical trials across different therapeutic areas.
• Recruit participants and obtain informed consent.
• Perform vital signs, phlebotomy, ECGs, and laboratory specimen processing.
• Manage regulatory documentation, study records, and site audits.
• Coordinate study activities from start to finish while working with investigators, sponsors, and monitors.
• Mentor junior staff and contribute to internal training.

Requirements

• Hands-on experience obtaining vital signs, performing phlebotomy, conducting ECGs, and processing laboratory specimens.
• Solid understanding of clinical site operations and the drug development process.
• CRC I: 1–3 years of experience in a clinical research setting at an investigative site working with participants.
• CRC II: At least 3 years of experience as a Clinical Research Coordinator at an investigative site working with participants.
• Strong written and verbal communication, attention to detail, and time-management skills.
• Experience with CTMS, eCRFs, and Microsoft Office tools.

Culture & Benefits

• Collaborative environment focused on initiative, adaptability, and continuous learning.
• Exposure to diverse trials and multiple therapeutic areas.
• Opportunities to work with investigators, sponsors, and clinical monitors.
• Potential incentive plans, bonuses, and health and welfare benefits may be available depending on the position.