Clinical Research Associate

ICON Clinical Research, LP

Taipei, Taiwan
Fully remote
Conduct site visits
Ensure protocol compliance
Maintain data integrity
As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials, ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • Conduct site visits
  • Ensure protocol compliance
  • Maintain data integrity
  • Resolve data queries
  • Prepare study documentation

Nice-to-have

  • Foster inclusive environment
  • Drive innovation and excellence
  • Advance innovative treatments
  • Work life balance opportunities

Key Requirements

  • Minimum 2 years experience CRA
  • In-depth knowledge ICH-GCP
  • Ability to travel 60%
  • Valid driver's license

Work Rights

Not specified

Tailored Resume

Cover Letter