Clinical Research Associate Ii

ICON

Shanghai, China
On-site
Clinical trial monitoring
Protocol compliance
Data integrity
ICON is seeking a Clinical Research Associate II for their Shanghai office to support clinical trials through monitoring, data analysis, and collaboration with site staff. The ideal candidate should possess a scientific degree, have at least 2 years of relevant experience, and be familiar with clinical trial processes and regulations

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.
  • In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance.

Matching Summary

Match Score: 85

ICON is seeking a Clinical Research Associate II for their Shanghai office to support clinical trials through monitoring, data analysis, and collaboration with site staff. The ideal candidate should possess a scientific degree, have at least 2 years of relevant experience, and be familiar with clinical trial processes and regulations.

Skills & Requirements

Must-have

  • clinical trial monitoring
  • protocol compliance
  • data integrity
  • patient safety
  • ICH-GCP guidelines

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • collaborative work environment

Key Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Associate
  • Willingness to travel as required (approximately 60%)

Work Rights

Not specified

Tailored Resume

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