Clinical Research Associate

ICON

Czech Republic
Coordinate clinical trial activities independently
Ensure compliance with regulatory requirements
Maintain study documentation and status reports
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
  • The Clinical Research Associate will coordinate and monitor clinical studies, ensuring patient safety and regulatory compliance.
  • ICON offers competitive salary and a range of benefits focused on well-being, including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.

Skills & Requirements

Must-have

  • Coordinate clinical trial activities independently
  • Ensure compliance with regulatory requirements
  • Maintain study documentation and status reports
  • Manage sponsor generated queries efficiently
  • Develop collaborative relationships with stakeholders
  • Ability to travel at least 60% internationally and domestically

Nice-to-have

  • Excellent written and verbal communication in English
  • Good social skills for timely query resolution
  • Inclusive and diverse work environment
  • Focus on well-being and work-life balance

Key Requirements

  • University degree in medicine, science, or equivalent
  • Knowledge of ICH-GCP guidelines
  • Valid driver’s license
  • Ability to travel at least 60% of the time

Work Rights

Not specified

Tailored Resume

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