Clinical Research Coordinator Ii (site Management Associate Ii)

ICON Clinical Research, LP

Munich, Germany
Ensure compliance with study protocols
Adhere to regulatory requirements
Follow good clinical practice (gcp)
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.
  • You will contribute to the efficiency of clinical research operations by providing advanced support to site management teams and fostering strong relationships with site personnel.
  • 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 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

  • Ensure compliance with study protocols
  • Adhere to regulatory requirements
  • Follow Good Clinical Practice (GCP)
  • Coordinate monitoring activities
  • Prepare and review regulatory documents
  • Track site performance metrics
  • Speak fluent German

Nice-to-have

  • Foster strong relationships with site personnel
  • Cross-functional team collaboration
  • Mentor junior staff

Key Requirements

  • Bachelor's degree in a relevant field
  • Experience in clinical research, site management, or monitoring
  • Solid understanding of clinical trial processes and GCP guidelines
  • Strong organizational and project management skills
  • Excellent analytical skills and attention to detail
  • Exceptional communication and interpersonal skills
  • Must be able to go to office in Munich

Work Rights

Not specified

Tailored Resume

Cover Letter