Cdc I

ICON Clinical Research, LP

Warsaw, Poland
Hybrid
Ecrf development assistance
Data validation specifications
Study specific procedures
As a Clinical Data Coordinator 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 Data Coordinator 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.
  • Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures.
  • 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 Clinical Data Coordinator 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

  • eCRF development assistance
  • data validation specifications
  • study specific procedures
  • review clinical and third-party data
  • issue clear, accurate, and concise queries
  • communicate effectively with peers
  • ensure study timelines are met

Nice-to-have

  • foster an inclusive environment
  • driving innovation and excellence
  • advancement of innovative treatments
  • diverse and dynamic team

Key Requirements

  • Master’s degree in a relevant field
  • Basic knowledge of clinical data management
  • Familiarity with data management software
  • Availability to start work at the beginning of July

Work Rights

Not specified

Tailored Resume

Cover Letter