Clinical Research Coordinator, On-Site, Bountiful, Utah

IQVIA; Bountiful (UT); On-site; USD 36,600 - 91,300; Full time

Job summary

IQVIA is seeking a Clinical Research Coordinator in Bountiful, Utah. This on-site position offers clinical research professionals hands-on experience and responsibilities across multiple trials and therapeutic areas.

You will manage trial activities, mentor junior staff, and work in a supportive team that values adaptability and continuous learning. The position is ideal for those looking to grow in clinical operations.

The base pay range for this role is $36,600 - $91,300 annually.

Qualifications

• Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens.
• Solid understanding of site operations and the drug development process.
• Minimum of 1-3 years for CRC I or 3 years as a Clinical Research Coordinator for CRC II.
• Strong written and verbal communication skills, with attention to detail and time management.

Responsibilities

• Manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish.
• Work closely with investigators, sponsors, and monitors while mentoring junior staff.

Skills

Clinical Skills

Site Operations Knowledge

Communication & Documentation

Technical Proficiency

Tools

CTMS

eCRFs

Microsoft Office

Job description

This is a fully on-site position in Bountiful, Utah.

Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands‑on responsibilities, and a collaborative team environment.

Why Avacare?

At Avacare, CRCs wear more hats than in traditional research settings. You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits. This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond.

What You’ll Gain

• Broadened Skill Set: Manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish.
• Professional Growth: Work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training.
• Collaborative Culture: Be part of a supportive team that values initiative, adaptability, and continuous learning.
• Global Impact: Experience the synergy of working within a local SMO backed by the resources and reach of a global CRO.

Qualifications

• Clinical Skills: Hands‑on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens.
• Site Operations Knowledge: Solid understanding of site operations and the drug development process.
• Experience:
• CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants.
• CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants.
• Communication & Documentation: Strong written and verbal communication skills, with attention to detail and time management.
• Technical Proficiency: Comfortable using CTMS, eCRFs, and Microsoft Office tools.

Whether you're early in your CRC journey or ready to take the next step, Avacare offers a unique environment where your contributions matter and your career can flourish.

The potential base pay range for this role, when annualized, is $36,600.00 - $91,300.00.

IQVIA is a proud equal‑opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.