Clinical Research Associate I

ICON

Sao Paulo, Brazil
Coordinate clinical trial activities
Ensure compliance with protocols and regulations
Maintain study documentation and reports
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, maintaining documentation, and ensuring patient safety through compliance with procedures and regulatory requirements.
  • 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
  • Ensure compliance with protocols and regulations
  • Maintain study documentation and reports
  • Develop relationships with clinical investigators
  • Travel at least 60% internationally and domestically

Nice-to-have

  • Excellent written and verbal communication in English
  • Good social skills for timely query resolution
  • Participate in feasibility studies and proposal reviews
  • Work independently and proactively

Key Requirements

  • University degree in medicine or science
  • 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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