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

1-3 years
$36,600.00 – $91,300.00
10 Nov. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Research Coordinator – On-Site (Salt Lake City, Utah)

Location: Salt Lake City, Utah
Employment Type: Full-Time | Office-Based
Requisition ID: R1510623
Experience Level: 1–3+ Years (Depending on CRC Level)

Position Overview

Avacare is seeking a skilled Clinical Research Coordinator (CRC) to support on-site clinical trial operations in Salt Lake City, Utah. This role is fully office-based and offers significant exposure to diverse therapeutic areas, complex clinical protocols, and end-to-end study coordination. Ideal for professionals looking to accelerate their clinical research career within a high-growth Site Management Organization (SMO).

At Avacare, CRCs manage broader responsibilities than in traditional research settings, providing a strong foundation for future advancement into clinical operations, monitoring, and site leadership roles.


Key Responsibilities

  • Coordinate 2–6 clinical trials varying in complexity, ensuring adherence to protocol and regulatory standards.

  • Conduct clinical procedures including vital signs, phlebotomy, ECGs, and lab specimen processing.

  • Lead participant recruitment, screening, informed consent, and visit scheduling.

  • Maintain accurate study documentation, regulatory files, and source records.

  • Serve as a primary point of contact for investigators, sponsors, monitors, and site staff.

  • Prepare for and support monitoring visits, audits, and inspections.

  • Mentor junior research staff and contribute to internal process improvement.

  • Utilize CTMS, eCRFs, and standard office software for data entry and tracking.


Required Qualifications

Clinical Expertise

  • Hands-on skills including blood draws, ECGs, vital signs collection, and lab sample handling.

Technical & Operational Knowledge

  • Understanding of clinical site operations, study workflows, and the drug development lifecycle.

  • Proficiency in CTMS platforms, eCRFs, and Microsoft Office tools.

Communication & Coordination

  • Strong written and verbal communication abilities.

  • High attention to detail, time management, and documentation accuracy.


Experience Requirements

  • CRC I: Minimum 1–3 years of experience working at a clinical investigative site with human research participants.

  • CRC II: Minimum 3+ years of experience specifically as a Clinical Research Coordinator at an investigative research site.


Why Work With Avacare?

  • Expanded Skill Development: Gain comprehensive exposure to site operations, clinical procedures, and multi-therapeutic trials.

  • Career Advancement: Opportunities to grow into senior CRC, clinical operations, or monitoring roles.

  • Collaborative Environment: Supportive team culture that values initiative and continuous learning.

  • Global Reach: Operate within a structured SMO while benefiting from the resources of a global CRO.


About IQVIA

IQVIA is a global leader in clinical research, healthcare analytics, and technology-enabled solutions. The organization supports the development and commercialization of innovative medical therapies that enhance patient outcomes worldwide.


Compensation

Annual Base Pay Range: $36,600.00 – $91,300.00
Actual compensation may vary based on experience, education, geographic location, and role-specific qualifications. Additional incentives and benefits may apply.


Apply Now to join Avacare and advance your clinical research career with a globally recognized organization.