Cdc I

ICON plc

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.
  • 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 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 data
  • issue data queries
  • clinical data management experience

Nice-to-have

  • foster inclusive environment
  • advance innovative treatments
  • collaborate with cross-functional teams
  • knowledge of regulatory guidelines

Key Requirements

  • Bachelor's degree in Life Sciences or Healthcare
  • Familiarity with data management software

Work Rights

Not specified

Tailored Resume

Cover Letter