Clinical Research Coordinator Ii (site Management Associate Ii)

ICON Clinical Research, LP

Munich, Germany
Site management associate ii
Clinical trial site management
Gcp guidelines compliance
As a Site Management Associate II at ICON, you will play a vital role in supporting the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines

Job Summary

  • As a Site Management Associate II at ICON, you will play a vital role in supporting the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
  • 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 we are dedicated to providing an inclusive and accessible environment for all candidates.

Matching Summary

As a Site Management Associate II at ICON, you will play a vital role in supporting the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

Skills & Requirements

Must-have

  • Site Management Associate II
  • Clinical trial site management
  • GCP guidelines compliance
  • Cross-functional team collaboration
  • Site performance tracking
  • Fluent German speaker

Nice-to-have

  • Fostering inclusive environment
  • Nurturing talent
  • Work-life balance opportunities
  • Mentoring junior staff

Key Requirements

  • Bachelor's degree in relevant field
  • Experience in clinical research
  • Solid understanding of clinical trial processes
  • Must be able to go to office in Munich

Work Rights

Not specified

Tailored Resume

Cover Letter