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

1-3 years
$36,600 – $91,300,
10 Nov. 21, 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 (On-Site)
Job Type: Full-Time
Job ID: R1510623
Work Model: Office-Based
Additional Locations Available

About the Role

Avacare, a leading Site Management Organization (SMO), is seeking a dedicated Clinical Research Coordinator (CRC) to support the successful execution of clinical trials across multiple therapeutic areas. This is a fully on-site role in Salt Lake City, Utah, designed for professionals who want to expand their clinical research experience and take ownership of key operational responsibilities.

This position offers extensive exposure to complex studies, direct interaction with participants, and hands-on involvement in regulatory, operational, and clinical activities. CRCs at Avacare gain broader responsibilities than traditional site roles, enabling accelerated professional growth.


Key Responsibilities

  • Coordinate and manage 2–6 clinical trials of varying complexity from initiation to close-out.

  • Support patient recruitment, conduct informed consent discussions, and maintain participant engagement throughout the study.

  • Perform essential clinical procedures including vital signs collection, ECGs, phlebotomy, and specimen processing.

  • Maintain accurate regulatory documentation, assist during site audits, and ensure compliance with all regulatory and GCP standards.

  • Work closely with investigators, sponsors, monitors, and cross-functional stakeholders to support operational efficiency.

  • Mentor junior team members and contribute to internal training initiatives.

  • Utilize CTMS, eCRFs, and digital tools to manage study data and documentation.

  • Collaborate within a supportive team culture that values continuous learning and proactive problem-solving.


Qualifications

Clinical Skills

  • Hands-on experience in vital signs collection, phlebotomy, ECGs, and laboratory specimen handling.

Operational Knowledge

  • Strong understanding of clinical site operations and the clinical trial process.

Experience Requirements

  • CRC I: Minimum 1–3 years of experience in a clinical research setting at an investigative site working directly with study participants.

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

Additional Requirements

  • Strong written and verbal communication skills with excellent documentation practices.

  • Effective time management and organizational skills.

  • Proficiency in CTMS, eCRFs, and Microsoft Office applications.

  • Ability to work collaboratively within a dynamic and fast-paced environment.


Why Join Avacare?

  • Broadened Skill Development: Gain extensive experience across diverse therapeutic areas and complex study designs.

  • Career Advancement: Work directly with investigators and sponsors, preparing you for progression into clinical operations, monitoring, and leadership roles.

  • Supportive Environment: Be part of a collaborative team that values initiative, adaptability, and continuous improvement.

  • Global Exposure: Benefit from the structure of a local SMO backed by global CRO capabilities.


About IQVIA

IQVIA is a global leader in advanced analytics, clinical research, and healthcare intelligence. The company supports the development and commercialization of innovative medical therapies that enhance patient outcomes and public health worldwide.


Compensation

The anticipated annual base pay range for this position is $36,600 – $91,300, with actual pay dependent on experience, qualifications, location, and work schedule. Additional compensation may include incentives, bonuses, and comprehensive health and welfare benefits.