Cra Ii

ICON

Kuala Lumpur, Malaysia
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.
  • The Clinical Research Associate II will conduct site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance and data integrity.
  • ICON offers competitive salary and a range of benefits focused on well-being, work-life balance, and inclusive culture.

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
  • 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 environment

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter