# Clinical Research Coordinator, On-Site, Bountiful, Utah

Hiring organization: [IQVIA](https://career.thegoodapps.co/organizations/iqvia)

Canonical page: https://career.thegoodapps.co/jobs/018c623d-8fd0-4d04-b472-49a79e200032

Listed on IQVIA's own careers site. Applications go to them directly.

- Employment type: full time
- Seniority: Entry
- Location: Bountiful, UT
- Salary: 36600 – 91300 USD per year

## Summary

This on-site clinical research coordinator role at an SMO offers hands-on experience managing multiple trials across different therapeutic areas, from patient recruitment through regulatory documentation. It suits someone looking to build broad expertise in trial operations while working closely with investigators and contributing to a collaborative team.

_Our summary, not IQVIA's wording._

## Skills named

Electrocardiogram (EKG/ECG), Microsoft Office, Phlebotomy, Vital Signs

## Required

- 1–3 years of clinical research experience at a clinical investigative site (CRC I level) or 3+ years as a Clinical Research Coordinator (CRC II level)
- Hands-on clinical skills including vital signs, phlebotomy, ECGs, and lab specimen processing
- Understanding of site operations and drug development process
- Strong written and verbal communication with attention to detail

## Nice to have

- Mentoring experience with junior staff
- Experience with internal training contribution

Apply on IQVIA's site: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Bountiful-UT-United-States-of-America/Clinical-Research-Coordinator--On-Site--Bountiful--Utah_R1513880-1