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Clinical Research Coordinator, On-Site, Springville, Utah

0-2 years
$36,600.00 - $91,300.00
10 Aug. 5, 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

Clinical Research Coordinator – Full-Time
Location: Springville, Utah (On-site)
Job Type: Full-Time | Office-Based
Requisition ID: R1488496
Company: IQVIA

Salary:
$36,600 – $91,300 annually
(Compensation may vary based on education, experience, skills, and location. Additional incentives and benefits may apply.)


Position Overview:
IQVIA is hiring a Clinical Research Coordinator (CRC) to support on-site clinical trial operations in Springville, Utah. In this role, you will collaborate with principal investigators and study teams to ensure protocol compliance, patient safety, and quality data collection, making a direct impact on clinical research and patient outcomes.


Key Responsibilities:

  • Coordinate and execute clinical research studies under a principal investigator

  • Serve as a backup CRC on other ongoing trials

  • Develop and implement effective patient recruitment strategies to meet enrollment goals

  • Obtain and document informed consent from study participants

  • Schedule and manage study visits and follow-up appointments

  • Collect patient medical histories and maintain source documentation

  • Administer investigational products/test articles

  • Handle data entry, query resolution, and manage clinical trial documentation

  • Collect, process, and ship lab specimens

  • Support pre-study, site qualification, initiation, monitoring, and close-out visits

  • Maintain compliance with IRB-approved protocols and GCP/ICH guidelines

  • Ensure participant safety and report adverse events appropriately

  • Order and maintain study materials and supplies

  • Travel to nearby clinic locations as needed


Qualifications:

  • Familiarity with GCP/ICH and regulatory guidelines

  • Prior experience as a Clinical Research Coordinator preferred

  • Clinical skills (vitals, phlebotomy, EKG) are a plus

  • Understanding of site operations and drug development processes

  • Strong written and verbal communication skills

  • Proficient with Microsoft Word and Excel

  • Detail-oriented and organized with a commitment to quality and compliance