Cra 2

ICON

US
Fully remote
Clinical trial site monitoring
Protocol compliance and patient safety
Data review and query resolution
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
  • As a Clinical Research Associate II, you will conduct site visits, ensure data integrity, and contribute to clinical trial documentation.
  • ICON offers competitive salary and benefits focused on well-being and work-life balance, including health insurance and retirement planning.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.

Skills & Requirements

Must-have

  • Clinical trial site monitoring
  • Protocol compliance and patient safety
  • Data review and query resolution
  • Collaborating with investigators and site staff
  • Ability to travel at least 60%

Nice-to-have

  • Strong organizational and communication skills
  • Attention to detail
  • Ability to work independently and collaboratively
  • Inclusive and accessible work environment

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum 2 years Clinical Research Associate experience
  • In-depth knowledge of clinical trial regulations and ICH-GCP guidelines
  • Valid driver’s license
  • Ability to travel internationally and domestically

Work Rights

Not specified

Tailored Resume

Cover Letter