Site Management Associate I

ICON

Sao Paulo, Brazil
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 additional 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 committed to providing a workplace free of discrimination and harassment.

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
  • data entry and tracking
  • cross-functional team collaboration
  • advanced level of English

Nice-to-have

  • training and development initiatives
  • inclusive and accessible environment
  • work life balance focus
  • diverse culture
  • operational efficiency

Key Requirements

  • Bachelor’s degree in relevant field
  • based in Brazil
  • global clinical research experience preferred
  • advanced English proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter