Clinical Research Associate

ICON Broadbean

Slovakia
Monitoring clinical trial sites
Strong organizational skills
Proficiency in clinical trial software
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials

Job Summary

  • As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials.
  • You will collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
  • ICON offers a range of benefits designed to support well-being and work-life balance opportunities.

Matching Summary

As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials.

Skills & Requirements

Must-have

  • Monitoring clinical trial sites
  • Strong organizational skills
  • Proficiency in clinical trial software

Nice-to-have

  • Excellent communication skills
  • Ability to influence compliance
  • Supportive team environment

Key Requirements

  • Advanced degree in life sciences
  • 3-6 years as a Clinical Research Associate
  • Ability to travel at least 60% of the time

Work Rights

Not specified

Tailored Resume

Cover Letter