Clinical Trial Assistance

ICON

Sao Paulo, Brazil
Clinical trial activities coordination
Site feasibility assessments
Study protocol compliance monitoring
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 assisting in planning, initiation, execution of clinical trial activities, site feasibility, site coordination, monitoring study progress, and documentation.
  • 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.

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

  • clinical trial activities coordination
  • site feasibility assessments
  • study protocol compliance monitoring
  • study documentation preparation
  • data collection quality assurance

Nice-to-have

  • strong organizational skills
  • effective communication skills
  • ability to work independently
  • collaborative team environment
  • attention to detail
  • task prioritization

Key Requirements

  • Bachelor's degree in life sciences or healthcare
  • previous clinical research experience preferred

Work Rights

Not specified

Tailored Resume

Cover Letter