Clinical Research Associate Ii

ICON Clinical Research, LP

Shenyang, China
On-site
Protocol compliance
Data integrity
Patient safety
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies

Job Summary

  • As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
  • You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
  • Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Matching Summary

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • protocol compliance
  • data integrity
  • patient safety
  • site qualification
  • study documentation

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • work life balance opportunities

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Minimum of 2 years experience as CRA
  • In-depth knowledge of clinical trial processes
  • ICH-GCP guidelines knowledge
  • Ability to work independently and collaboratively
  • Willingness to travel approximately 60%

Work Rights

Not specified

Tailored Resume

Cover Letter