Clinical Research Associate, Sponsor Dedicated

ICON Broadbean

Multiple Locations
Clinical trial monitoring
Data integrity management
Site qualification visits
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 the trial process.
  • ICON fosters an inclusive environment that rewards high performance and nurtures talent.

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 qualification visits

Nice-to-have

  • Strong communication skills
  • Ability to work independently
  • Experience with electronic data capture

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

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