Clinical Research Coordinator, On-Site, Salt Lake City, Utah

IQVIASalt Lake City, UT
$36,600 - $91,300Onsite

About The Position

This is a fully on-site position in Salt Lake City, Utah. 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. 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. 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.

Requirements

  • Hands-on experience in obtaining vital signs
  • Performing phlebotomy
  • Conducting ECGs
  • Processing lab specimens
  • Solid understanding of site operations and the drug development process
  • 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
  • Strong written and verbal communication skills
  • Attention to detail
  • Time management
  • Comfortable using CTMS, eCRFs, and Microsoft Office tools

Responsibilities

  • Manage 2–6 trials of varying complexity
  • Perform clinical procedures
  • Lead study coordination from start to finish
  • Work closely with investigators, sponsors, and monitors
  • Mentor junior staff
  • Contribute to internal training
  • Patient recruitment
  • Informed consent
  • Regulatory documentation
  • Site audits

Benefits

  • Incentive plans
  • Bonuses
  • Range of health and welfare benefits
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