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 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
Manage site support activities
Prepare regulatory and site documents
Track site activation tasks
Assemble submission packages
Ensure Critical Document Package accuracy
Coordinate translations
Enter progress data into tracking systems
Nice-to-have
Foster inclusive environment
Contribute to quality improvement
Proactive service-focused mindset
Collaborate with cross-functional teams
Key Requirements
Bachelor's degree in life sciences, healthcare, business, or related field
3-6 years of experience in Clinical Research environment
Relevant experience in site support or clinical administration
Good understanding of clinical trial processes, GCP, and site documentation