Site Management Associate I

ICON Clinical Research, LP

Sao Paulo, Brazil
Assisting site monitoring activities
Ensuring compliance with study protocols
Maintaining operational efficiency
As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintaining high standards of operational efficiency

Job Summary

  • As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintaining high standards of operational efficiency.
  • You will contribute to the success of clinical research by providing essential administrative and logistical support to site management teams.
  • Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Matching Summary

As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintaining high standards of operational efficiency.

Skills & Requirements

Must-have

  • Assisting site monitoring activities
  • Ensuring compliance with study protocols
  • Maintaining operational efficiency
  • Providing administrative support
  • Providing logistical support

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Shaping the future of clinical development
  • Enhancing knowledge and skills

Key Requirements

  • Bachelor’s degree in relevant field
  • Advanced level of English
  • Based in Brazil

Work Rights

Not specified

Tailored Resume

Cover Letter