As a Site Management Associate I, 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, 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.
Your responsibilities include assisting in the monitoring of clinical trial sites, supporting site management activities, collaborating with cross-functional teams, and maintaining accurate records.
ICON offers a competitive salary, a range of additional benefits focused on well-being and work-life balance, including health insurance, retirement planning, and a Global Employee Assistance Programme.
Matching Summary
As a Site Management Associate I, 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
French language proficiency
Portuguese language proficiency
English language proficiency
Clinical trial site monitoring
Adherence to study protocols
Good Clinical Practice (GCP)
Nice-to-have
Organizational skills and attention to detail
Collaborative team environment
Life sciences background
Healthcare administration background
Clinical research background
Key Requirements
Bachelor's degree in relevant field
Advanced level Portuguese, French, and English
Experience in clinical research preferred
Experience in site management preferred
Experience in related administrative roles preferred