Clinical Research Associate I Or Ii

ICON

Sao Paulo, Brazil
Clinical trial monitoring visits
Protocol compliance and data integrity
Site qualification and initiation
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 role involves conducting site visits, ensuring protocol compliance, and collaborating with site staff to facilitate smooth study conduct.
  • 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 committed to innovation and excellence.

Skills & Requirements

Must-have

  • Clinical trial monitoring visits
  • Protocol compliance and data integrity
  • Site qualification and initiation
  • Patient safety management
  • Travel up to 60% internationally and domestically
  • Valid driver’s license

Nice-to-have

  • Strong organizational skills
  • Effective communication skills
  • Ability to work independently and collaboratively
  • Attention to detail

Key Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • Experience as a Clinical Research Associate with onsite monitoring visits
  • Knowledge of clinical trial processes, regulations, and ICH-GCP guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter