Clinical Trial Associate - Study Start Up

ICON Broadbean

Sao Paulo, Brazil
Fully remote
Clinical trial documentation management
Regulatory compliance knowledge
Cross-functional team collaboration
As a Clinical Trial Associate at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials

Job Summary

  • As a Clinical Trial Associate at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials.
  • You will contribute to the tracking and reporting of clinical trial metrics and milestones.
  • ICON offers a range of additional benefits focused on well-being and work-life balance opportunities.

Matching Summary

As a Clinical Trial Associate at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials.

Skills & Requirements

Must-have

  • Clinical trial documentation management
  • Regulatory compliance knowledge
  • Cross-functional team collaboration

Nice-to-have

  • Strong interest in clinical research
  • Excellent organizational skills
  • Attention to detail

Key Requirements

  • Bachelor's degree in a scientific field
  • Prior experience in clinical research
  • English proficiency at intermediate level

Work Rights

Not specified

Tailored Resume

Cover Letter