Clinical Research Associate

ICON plc

Missouri, United States
On-site monitoring experience
Site compliance with regulations
Proficient in clinical systems
ICON plc is a world-leading healthcare intelligence and clinical research organization

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization.
  • You will serve as the primary point of contact between investigational sites and the sponsor.
  • ICON offers a range of additional benefits focused on well-being and work-life balance.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization.

Skills & Requirements

Must-have

  • On-site monitoring experience
  • Site compliance with regulations
  • Proficient in clinical systems

Nice-to-have

  • Collaborative team player
  • Problem-solver
  • Clear communicator

Key Requirements

  • Bachelor’s degree in Life Sciences
  • 2+ years of on-site monitoring experience
  • Eligible to work in United States

Work Rights

Not specified

Tailored Resume

Cover Letter