Manage multiple clinical trials by coordinating patient recruitment, informed consent, and regulatory documentation. Perform clinical procedures and collaborate with investigators and sponsors to ensure successful trial execution.
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.
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 [https://jobs.iqvia.com/]
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 [https://jobs.iqvia.com/eoe]
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.
Requires 1-3 years of experience for CRC I or 3+ years for CRC II in a clinical investigative site. Candidates must possess hands-on clinical skills such as phlebotomy and ECGs, along with proficiency in CTMS and eCRFs.
Market context
Clinical Research Coordinator roles in Utah are often tied to active clinical trial sites, where demand tends to follow study volume and the need for coordinators who can manage patient visits, documentation, and protocol compliance. This role is competitive because employers look for hands-on clinical skills like phlebotomy and ECGs, plus experience with CTMS and eCRFs; job requirements and benefits here are AI-summarized from the original posting to save you research time. If you are considering applying, review your site-based research experience and be ready to show how you handled data accuracy, patient coordination, and regulatory tasks.
