Clinical Research Coordinator, On-site, South Ogden, Ut

IQVIA UK

South Ogden, Utah, US
Base: $36,600.00 - $106,800.00; bonus/equity: ince...
Review study protocols and case report forms
Collect and submit regulatory ethics documentation
Recruit and screen patients for clinical trials
The role involves performing a variety of complex clinical research procedures including ECG, sample collection, and cardiac telemetry monitoring according to strict protocols

Job Summary

  • The role involves performing a variety of complex clinical research procedures including ECG, sample collection, and cardiac telemetry monitoring according to strict protocols.
  • Candidates will be responsible for recruiting and screening patients, maintaining subject logs, and ensuring all regulatory documentation is submitted to the FDA and other bodies.
  • IQVIA offers a competitive base pay range of $36,600.00 to $106,800.00 along with potential incentive plans and comprehensive health benefits.

Matching Summary

The role involves performing a variety of complex clinical research procedures including ECG, sample collection, and cardiac telemetry monitoring according to strict protocols.

Salary

Base: $36,600.00 - $106,800.00; Bonus/Equity: Incentive plans and bonuses may be offered; Benefits: Range of health and welfare benefits included

Skills & Requirements

Must-have

  • Review study protocols and Case Report Forms
  • Collect and submit regulatory ethics documentation
  • Recruit and screen patients for clinical trials
  • Perform ECG, spirometry, and vital signs monitoring
  • Maintain source documentation and study logs
  • Handle lab testing and specimen collection logistics

Nice-to-have

  • Excellent interpersonal skills with team members
  • Ability to troubleshoot study-related questions
  • Experience training new site staff members
  • Strong attention to detail in data entry
  • Effective working relationships with investigators

Key Requirements

  • Bachelor's Degree or High School Diploma
  • 3 years relevant work experience in clinical environment
  • Working knowledge of Good Clinical Practices (GCP)
  • Skill in intravenous catheter insertion and spirometry
  • Proficiency with MS Windows and Office applications

Work Rights

Not specified

Tailored Resume

Cover Letter