On-Site Clinical Research Coordinator — Diverse Trials & Growth

Regulatory Jobs; Bountiful (UT); On-site; USD 37,000 - 91,000; Full time

Job summary

Avacare in Utah is seeking Clinical Research Coordinators for on-site roles at a busy SMO environment. You’ll gain exposure to multiple trials, perform essential clinical procedures, and coordinate study activities from start to finish.

CRC I/II experience ranges 1–3 years; strong documentation, CTMS/eCRF proficiency, and clear communication are valued. Base pay ranges publicly from $36,600 to $91,300 annually, with potential bonuses and benefits depending on qualifications.

Qualifications

• Hands-on experience in vital signs, phlebotomy, ECGs, and lab specimens.
• Solid understanding of site operations and drug development processes.
• CRC I: 1–3 years at a clinical investigative site; CRC II: 3+ years in a similar role.

Responsibilities

• Obtain vital signs, perform phlebotomy, ECGs, and process labs.
• Manage trial activities and ensure accurate regulatory documentation.
• Coordinate patient recruitment, informed consent, and study visits.
• Support site audits and maintain CTMS/eCRF entries with precision.

Skills

Clinical Skills

Site Operations

Communication

Documentation

Technical Proficiency

Tools

CTMS

eCRFs

Microsoft Office

Job description

Avacare in Utah is seeking Clinical Research Coordinators for on-site roles at a busy SMO environment. You’ll gain exposure to multiple trials, perform essential clinical procedures, and coordinate study activities from start to finish.

CRC I/II experience ranges 1–3 years; strong documentation, CTMS/eCRF proficiency, and clear communication are valued. Base pay ranges publicly from $36,600 to $91,300 annually, with potential bonuses and benefits depending on qualifications.