Cra Standard

ICON

Guangzhou, , China
Clinical trial monitoring and site visits
Protocol compliance and data integrity
Travel at least 60% internationally and domestically
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 qualification, initiation, monitoring, and close-out visits while ensuring patient safety and data quality.
  • ICON offers competitive salaries and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

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 monitoring and site visits
  • Protocol compliance and data integrity
  • Travel at least 60% internationally and domestically
  • Valid driver’s license required
  • Data review and query resolution

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-related field
  • Minimum 2 years Clinical Research Associate experience
  • In-depth knowledge of clinical trial processes and ICH-GCP guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter