Clinical Research Associate, Sponsor Dedicated

ICON plc

Multiple Locations
Clinical trial monitoring
Data integrity management
Site management skills
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.
  • As a CRA, you will conduct site visits and ensure protocol compliance throughout clinical trials.
  • ICON offers a range of benefits designed to support well-being and work-life balance.

Matching Summary

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

Skills & Requirements

Must-have

  • Clinical trial monitoring
  • Data integrity management
  • Site management skills

Nice-to-have

  • Strong communication skills
  • Ability to work independently
  • Collaborative team player

Key Requirements

  • Bachelor's degree in a scientific field
  • Minimum of 2 years as a Clinical Research Associate
  • In-depth knowledge of ICH-GCP guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter