Cra Ii

ICON

Taipei, Taiwan
Fully remote
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 in clinical development

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence in clinical development.
  • The role involves pivotal responsibilities in designing and analyzing clinical trials, interpreting complex medical data, and advancing innovative treatments and therapies.
  • ICON offers competitive salaries and a range of benefits focused on well-being and work-life balance, including various annual leave entitlements, 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 in clinical development.

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 required

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 field
  • Minimum 2 years Clinical Research Associate experience
  • Knowledge of clinical trial processes and regulations
  • Ability to travel at least 60%
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter