Research Coordinator

IQVIA

Base: $43,400.00 - $108,200.00 annualized; bonus/e...
Protocol compliance with federal regulations
Informed consent process management
Patient eligibility assessment and screening
The Research Coordinator advocates for patient safety and protocol integrity while ensuring effective conduct of clinical trials

Job Summary

  • The Research Coordinator advocates for patient safety and protocol integrity while ensuring effective conduct of clinical trials.
  • Responsibilities include managing informed consent processes, assessing patient eligibility, and coordinating study-specific events and visits.
  • IQVIA offers a mission-driven environment valuing collaboration, precision, and excellence in accelerating medical treatment development.

Matching Summary

The Research Coordinator advocates for patient safety and protocol integrity while ensuring effective conduct of clinical trials.

Salary

Base: $43,400.00 - $108,200.00 annualized; Bonus/Equity: Dependent on position offered; Benefits: Health and welfare and/or other benefits available

Skills & Requirements

Must-have

  • Protocol compliance with federal regulations
  • Informed consent process management
  • Patient eligibility assessment and screening
  • Adverse event reporting to IRB
  • Electronic data capture entry

Nice-to-have

  • Oncology clinical trial experience preferred
  • Strong interdisciplinary communication skills
  • Supportive team culture commitment
  • Patient education and advocacy focus

Key Requirements

  • 5 or more years of experience
  • Current Texas or Virginia Registered Nursing License for RNs
  • Bachelor's degree required for non-RNs
  • Knowledge of standard research and oncology care practices

Work Rights

Not specified

Tailored Resume

Cover Letter