Cra 2

ICON

Multiple Locations
Clinical trial site monitoring
Protocol compliance and patient safety
Data integrity and query resolution
CRA II ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence

Job Summary

  • CRA II ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
  • The role involves conducting site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance and patient safety.
  • ICON offers competitive salary and benefits focused on well-being and work-life balance, including health insurance, retirement planning, and a global employee assistance program.

Matching Summary

CRA II 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 integrity and query resolution
  • Collaboration with investigators and site staff
  • Travel at least 60% internationally and domestically

Nice-to-have

  • Strong organizational and communication skills
  • Ability to work independently and collaboratively
  • Attention to detail
  • Inclusive and diverse work culture

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum 2 years Clinical Research Associate experience
  • In-depth knowledge of clinical trial processes and ICH-GCP guidelines
  • Valid driver’s license
  • Good level of English language

Work Rights

Not specified

Tailored Resume

Cover Letter