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.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are 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
Clinical trial site management
Ensure compliance with GCP
Coordinate monitoring activities
Track site performance metrics
Excellent English and French required
Nice-to-have
Foster inclusive environment
Drive innovation and excellence
Support junior staff development
Focus on well-being and work-life balance
Key Requirements
Bachelor's degree in relevant field
Experience in clinical research
Solid understanding of clinical trial processes
Strong organizational and project management skills
Excellent analytical skills and attention to detail
Exceptional communication and interpersonal skills