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ICON Broadbean

Buenos Aires, Argentina
Fully remote
Oversee and coordinate clinical trials
Ensure regulatory compliance
Collect and analyze data
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization focused on 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 a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

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

Skills & Requirements

Must-have

  • Oversee and coordinate clinical trials
  • Ensure regulatory compliance
  • Collect and analyze data
  • Maintain study documentation
  • Patient safety compliance

Nice-to-have

  • Foster inclusive environment
  • Drive innovation and excellence
  • Shape future of clinical development
  • Collaborative relationships
  • Work-life balance opportunities

Key Requirements

  • Bachelor's degree completed
  • At least 1 year of experience as CRA
  • Knowledge of ICH-GCP guidelines
  • Ability to travel at least 60%

Work Rights

Not specified

Tailored Resume

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