Site Management Associate I

ICON Clinical Research, LP

Buenos Aires, Argentina
Fully remote
Site monitoring activities
Study protocols adherence
Regulatory requirements
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.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

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

  • site monitoring activities
  • study protocols adherence
  • regulatory requirements
  • Good Clinical Practice (GCP)
  • documentation preparation
  • data entry
  • tracking site performance

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • work life balance opportunities
  • inclusion & belonging are fundamental

Key Requirements

  • Bachelor’s degree in relevant field
  • Some experience in clinical research
  • Basic knowledge of clinical trial processes

Work Rights

Not specified

Tailored Resume

Cover Letter