Site Management Associate

ICON

Mexico City, Mexico
Fully remote
Site monitoring activities
Compliance with study protocols
Good clinical practice (gcp) guidelines
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.
  • ICON offers a range of benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and the company is dedicated to providing an inclusive and accessible environment for all candidates.

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
  • Compliance with study protocols
  • Good Clinical Practice (GCP) guidelines
  • Documentation preparation and data entry
  • Collaboration with cross-functional teams

Nice-to-have

  • Strong organizational skills
  • Attention to detail
  • Excellent communication skills
  • Team collaboration
  • Basic clinical trial process knowledge

Key Requirements

  • Bachelor’s degree in life sciences or related field
  • Experience with global clinical trial teams
  • Experience as Clinical Trial Assistant or Project Manager Assistant

Work Rights

Not specified

Tailored Resume

Cover Letter