Clinical Research Associate I

ICON

Buenos Aires, Argentina
Fully remote
Coordinate clinical trial activities independently
Ensure compliance with regulatory requirements
Maintain study documentation and reporting
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.
  • The role involves coordinating study setup and monitoring, managing study documentation, and ensuring patient safety through compliance with protocols and regulations.
  • ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.

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

  • Coordinate clinical trial activities independently
  • Ensure compliance with regulatory requirements
  • Maintain study documentation and reporting
  • Develop collaborative stakeholder relationships
  • Travel at least 60% internationally and domestically

Nice-to-have

  • Good social skills for timely query resolution
  • Strong written and verbal communication in English
  • Ability to review and evaluate medical data

Key Requirements

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

Work Rights

Not specified

Tailored Resume

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