Cra Ii

ICON Clinical Research, LP

Shanghai, China
Conduct site visits
Ensure protocol compliance
Data integrity and patient safety
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
  • Data integrity and patient safety
  • Collaborate with investigators
  • Resolve data queries
  • Prepare study documentation

Nice-to-have

  • Foster inclusive environment
  • Drive innovation and excellence
  • Advance innovative treatments
  • Nurture talent
  • Focus on well-being

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum 2 years CRA experience
  • Knowledge of clinical trial regulations
  • ICH-GCP guidelines knowledge
  • Ability to travel 60% of the time
  • Valid driver's license

Work Rights

Not specified

Tailored Resume

Cover Letter