Cdc Ii

ICON

Multiple Locations
On-site
Clinical trial data review
Ecoa/external data reconciliation
Sae reconciliation
ICON plc is seeking a CDC II to design and analyze clinical trials, focusing on the interpretation of complex medical data. The ideal candidate will have relevant experience in clinical data management and a strong understanding of clinical trial processes

Job Summary

  • As a CDC II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
  • Your role will involve delivering clinical data management work to a high standard, working closely with your team and stakeholders.
  • ICON offers a competitive salary, various annual leave entitlements, a range of health insurance offerings, competitive retirement planning, and a Global Employee Assistance Programme.

Matching Summary

Match Score: 85

ICON plc is seeking a CDC II to design and analyze clinical trials, focusing on the interpretation of complex medical data. The ideal candidate will have relevant experience in clinical data management and a strong understanding of clinical trial processes.

Skills & Requirements

Must-have

  • Clinical trial data review
  • eCOA/external data reconciliation
  • SAE reconciliation
  • Data cleaning plan components
  • eTMF documentation

Nice-to-have

  • Mentoring data coordinators
  • Inspection readiness activities
  • Study data collection tools setup

Key Requirements

  • Bachelor's degree in Life Sciences or Healthcare
  • 2-5 years relevant work experience
  • Experience with electronic data collection systems
  • Knowledge of FDA and ICH regulations

Work Rights

Not specified

Tailored Resume

Cover Letter