Cdc Ii

ICON Clinical Research, LP

Fully remote
Clinical trial data review
Ecoa/external data management
Sae reconciliation
Your role will involve delivering clinical data management work to a high standard, working closely with your team and stakeholders

Job Summary

  • Your role will involve delivering clinical data management work to a high standard, working closely with your team and stakeholders.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities.
  • ICON is committed to providing a workplace free of discrimination and harassment, and all qualified applicants will receive equal consideration for employment.

Matching Summary

Your role will involve delivering clinical data management work to a high standard, working closely with your team and stakeholders.

Skills & Requirements

Must-have

  • clinical trial data review
  • eCOA/external data management
  • SAE reconciliation
  • data cleaning plan components
  • eTMF documentation

Nice-to-have

  • vendor and CRO liaison
  • inspection readiness activities
  • mentoring data coordinators

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