Clinical Trial Assistance

ICON plc

Sao Paulo, Brazil
Clinical trial execution
Site feasibility assessments
Compliance with study protocols
As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies

Job Summary

  • As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.

Matching Summary

As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • clinical trial execution
  • site feasibility assessments
  • compliance with study protocols
  • monitoring study progress
  • preparation of study documentation

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • work independently and collaboratively
  • attention to detail and prioritization

Key Requirements

  • Bachelor's degree in life sciences or healthcare
  • Previous experience in clinical research preferred
  • Ability to work independently and collaboratively

Work Rights

Not specified

Tailored Resume

Cover Letter