Clinical Research Associate

ICON Clinical Research, LP

Czech Republic
Overseeing and coordinating clinical trials
Ensuring compliance with regulations
Collecting and analyzing critical data
ICON plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment driving innovation and excellence.
  • As a Clinical Research Associate, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.
  • ICON offers competitive salary, a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and a global employee assistance program.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment driving innovation and excellence.

Skills & Requirements

Must-have

  • overseeing and coordinating clinical trials
  • ensuring compliance with regulations
  • collecting and analyzing critical data
  • ICH-GCP guidelines knowledge
  • review and evaluate medical data

Nice-to-have

  • foster an inclusive environment
  • driving innovation and excellence
  • strong collaborative relationships
  • patient safety focus

Key Requirements

  • University degree in medicine, science, or equivalent
  • Excellent written and verbal communication in English
  • Ability to travel at least 60% of the time
  • Valid drivers license

Work Rights

Not specified

Tailored Resume

Cover Letter