Instagram
youtube
Facebook

Clinical Research Coordinator, On-Site

1-3 years
$36,600 – $91,300
10 July 16, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Job Title:

Clinical Research Coordinator – On-site | Bountiful, Utah


Job Summary:

IQVIA is seeking a Clinical Research Coordinator for a full-time, on-site role in Bountiful, Utah. This position is integral to the success of clinical trials, supporting protocol execution, patient safety, and data accuracy. Ideal for individuals with strong interpersonal skills, attention to detail, and prior clinical research or healthcare experience, this role ensures compliance with GCP, ICH, and FDA regulations while contributing to meaningful clinical outcomes.


Key Responsibilities:

  • Coordinate 1–3 clinical studies of low to medium complexity under oversight

  • Support other studies as a backup CRC as needed

  • Develop and implement patient recruitment strategies to meet enrollment targets

  • Obtain informed consent and manage patient interactions

  • Maintain effective communication with study teams

  • Perform scheduling, vitals collection, phlebotomy, EKG, and source documentation

  • Manage investigational product inventory and administration

  • Support data entry, query resolution, and document review

  • Coordinate study-related procedures, visits, and follow-up

  • Handle specimen collection, processing, and shipment

  • Assist in site qualification, monitoring, and close-out visits

  • Ensure safety monitoring and adverse event reporting

  • Maintain compliance with IRB protocols and SOPs


Required Skills & Qualifications:

  • Prior Clinical Research Coordinator experience preferred

  • Working knowledge of GCP/ICH regulatory standards

  • Experience in clinical procedures (e.g., vitals, EKG, phlebotomy)

  • Strong knowledge of clinical trial site operations

  • Familiarity with clinical trial documentation and processes

  • Excellent communication and team coordination skills

  • Proficiency in Microsoft Word, Excel

  • Bachelor's degree preferred


Perks & Benefits:

  • Competitive annual salary: $36,600 – $91,300

  • Performance-based incentives and bonus eligibility

  • Full range of health and welfare benefits

  • Career growth opportunities with a global CRO leader

  • Supportive team environment with leading-edge training


Company Overview:

IQVIA is a global leader in clinical research, healthcare technology, and real-world evidence. We support the life sciences industry in accelerating clinical development, optimizing commercialization, and improving patient outcomes through innovative data-driven insights.


Work Mode:

On-site – Bountiful, Utah


Call-to-Action:

Be part of a mission-driven team that transforms patient care through research. If you're ready to advance your clinical career with a global leader, apply now for the Clinical Research Coordinator role at IQVIA in Bountiful, Utah..