Site Management Associate

ICON Clinical Research, LP

Multiple Locations
Fully remote
Assisting in site monitoring
Ensuring adherence to protocols
Maintaining accurate records
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

  • Assisting in site monitoring
  • Ensuring adherence to protocols
  • Maintaining accurate records
  • Collaborating with cross-functional teams

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Enhancing knowledge and skills
  • Supporting well-being and work-life balance

Key Requirements

  • Bachelor's degree in a relevant field
  • Some experience in clinical research
  • Strong organizational skills and attention to detail
  • Basic knowledge of clinical trial processes

Work Rights

Not specified

Tailored Resume

Cover Letter