Clinical Research Associate Ii

ICON

Shenyang, China
On-site
Protocol compliance
Data integrity
Patient safety
ICON is seeking a Clinical Research Associate II to contribute to clinical trial monitoring in Shenyang, China. The ideal candidate will have at least two years of experience in clinical research, strong organizational skills, and a willingness to travel

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 to contribute to clinical trial monitoring in Shenyang, China. The ideal candidate will have at least two years of experience in clinical research, strong organizational skills, and a willingness to travel.

Skills & Requirements

Must-have

  • protocol compliance
  • data integrity
  • patient safety
  • site qualification
  • site initiation
  • site monitoring
  • site close-out visits

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • advance innovative treatments

Key Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Ability to work independently and collaboratively
  • Willingness to travel as required (approximately 60%)

Work Rights

Not specified

Tailored Resume

Cover Letter