Site Management Associate Ii With French

ICON

Multiple Locations
Clinical trial site coordination
Regulatory compliance with gcp
Site performance tracking and reporting
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 benefits focused on well-being and work-life balance including health insurance, retirement planning, and a global employee assistance program.
  • ICON is dedicated to providing an inclusive and accessible environment for all candidates and is committed to a workplace free of discrimination and harassment.

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

  • Clinical trial site coordination
  • Regulatory compliance with GCP
  • Site performance tracking and reporting
  • Fluent English and French
  • Cross-functional team collaboration

Nice-to-have

  • Mentoring junior staff
  • Strong organizational skills
  • Analytical skills and attention to detail
  • Inclusive and diverse work culture

Key Requirements

  • Bachelor’s degree in relevant field
  • Experience in clinical research or site management
  • Solid understanding of clinical trial processes and GCP
  • Excellent English and French language skills

Work Rights

Not specified

Tailored Resume

Cover Letter