As a Site Specialist II at ICON, you will independently manage a range of site support activities, acting as a key operational contact for sites and contribute to efficient study start-up and maintenance
Job Summary
As a Site Specialist II at ICON, you will independently manage a range of site support activities, acting as a key operational contact for sites and contribute to efficient study start-up and maintenance.
Support preparation, process and tracking of regulatory and site level critical documents and of site activation tasks required for study site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable regulations/guidelines and the principles of ICH/GCP.
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 Specialist II at ICON, you will independently manage a range of site support activities, acting as a key operational contact for sites and contribute to efficient study start-up and maintenance.
Skills & Requirements
Must-have
site support activities
regulatory and site level critical documents
study site activation
ICH/GCP
Critical Document Package (CDP)
Trial Master File (TMF) documents
Nice-to-have
culture of quality and process improvement
proactive, service-focused mindset
collaboration with cross-functional teams
inclusive environment
Key Requirements
Bachelor's degree in life sciences, healthcare, business, or a related field
3-6 years of experience in a Clinical Research environment
Relevant experience in site support, clinical administration, or similar roles
Good understanding of clinical trial processes, GCP, and site documentation requirements