New · posted Nov 1
IQVIA · Pharmaceuticals
Clinical Research Coordinator
- Bountiful, UT
- On-site
- Full-time
- Associate & Specialist
The role
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.
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.
What you need
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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $36,600.00 - $91,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
Pay and benefits
$36,600 – $91,300 a year
Employer providedHealth and welfare benefits
Incentive plans
Bonuses
Where you'll work
Bountiful, UTOn-siteOpen in Maps (opens in a new tab)
More jobs in Bountiful, UT
From the posting
About IQVIA
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.
Equal opportunity, accessibility and legal noticesIQVIA's statements, word for word
IQVIA is proud to be an 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. https://jobs.iqvia.com/eoe
Job intelligence
The context around this role
Live data · November 1, 2026
Salary intelligence
How the pay compares
This role's midpoint is 42% below the US median for Clinical Research roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US56 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $36,600 | — | $91,300 |
| All US (middle half) | $80,000 | $110,000 | $127,875 |
This role: IQVIA's own published range. Comparisons: the base pay employers published on open Clinical Research roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Research
The general path across 193 open Clinical Research roles on Regulatory Jobs, with the titles they carry most. Not IQVIA's own promotion track.
Career resources on Clinical Research
Skills DNA
What this role leans on
How many of the posting's 14 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct6
- Collaboration and leadership5
- Documentation and SOPs2
- Investigations and CAPA2
- Validation and qualification1
- Data and digital systems1
Company hiring pulse
IQVIA on Regulatory Jobs
- 83
- Open roles
- 59
- Distinct roles
- 26
- Locations
By discipline
- Clinical72 87%
- Regulatory7 8%
- Quality4 5%
By level
- Associate & Specialist43 52%
- Manager15 18%
- Senior & Principal15 18%
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Clinical Research Coordinator at IQVIA
Open until filled. $37K–$91K a year, employer provided.