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ICON

Shenyang, China
Clinical trial site monitoring
Protocol compliance and data integrity
Ich-gcp guidelines knowledge
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 role involves conducting site visits, ensuring patient safety, and collaborating with site staff to facilitate clinical trials.
  • 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 data integrity
  • ICH-GCP guidelines knowledge
  • Travel up to 60% internationally and domestically
  • Valid driver’s license

Nice-to-have

  • Strong organizational skills
  • Effective 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
  • Knowledge of clinical trial processes and regulations
  • Valid driver’s license
  • Ability to travel at least 60%

Work Rights

Not specified

Tailored Resume

Cover Letter