Cdc I

ICON plc

Warsaw, Poland
Hybrid
Ecrf development
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
  • Data Validation Specifications
  • Study Specific Procedures
  • review clinical data
  • issue queries to sites

Nice-to-have

  • fast-paced environment
  • collaborate with cross-functional teams
  • inclusive environment
  • advancement of innovative treatments

Key Requirements

  • Bachelor's degree in Life Sciences or Healthcare
  • Basic knowledge of clinical data management
  • Familiarity with data management software
  • Regulatory guidelines knowledge is a plus

Work Rights

Not specified

Tailored Resume

Cover Letter