# Clinical Research Coordinator

**Company**: Avacare
**Location**: Bountiful, UT
**Work arrangement**: onsite
**Experience**: mid
**Job type**: full-time
**Salary**: $36,600.00 - $91,300.00
**Category**: Research
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Bountiful-UT-United-States-of-America/Clinical-Research-Coordinator--On-Site--Bountiful--Utah_R1513880-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_b06f47e4-e91

## Description

Join Avacare, a dynamic Site Management Organization (SMO), as a Clinical Research Coordinator (CRC) in Bountiful, Utah. You'll gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment.

As a CRC, you'll wear multiple hats, gaining experience across various therapeutic areas, managing complex protocols, and taking ownership of key trial activities, including patient recruitment, informed consent, regulatory documentation, and site audits.

**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 a 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.

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

## Skills

### Required
- CTMS
- eCRFs
- Microsoft Office
- clinical research
- phlebotomy
- ECGs
- lab specimens

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