In-house Clinical Research Associate

ICON

Sao Paulo, Brazil
Hybrid
Clinical trial activities coordination
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 benefits focused on well-being and work-life balance, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
  • ICON is dedicated to providing an inclusive and accessible environment, committed to a workplace free of discrimination and harassment, and encourages all qualified applicants to apply regardless of whether they meet all requirements.

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 activities coordination
  • Site feasibility assessments
  • Compliance with study protocols
  • Monitoring study progress
  • Study documentation preparation

Nice-to-have

  • Strong organizational skills
  • Effective communication skills
  • Ability to work independently
  • Collaborative team player
  • Attention to detail

Key Requirements

  • Bachelor's degree in life sciences or healthcare
  • English proficiency minimum intermediate
  • Previous clinical research experience preferred

Work Rights

Not specified

Tailored Resume

Cover Letter