As a Site Specialist I at ICON, you will support investigator sites with key administrative and operational activities to help ensure clinical trials run smoothly, efficiently, and in compliance with applicable regulations
Job Summary
As a Site Specialist I at ICON, you will support investigator sites with key administrative and operational activities to help ensure clinical trials run smoothly, efficiently, and in compliance with applicable regulations.
Support Site Partners to collect, review, organize and assemble initial start-up and maintenance submission packages to Central EC/IRB, Local EC/IRB, Competent Authorities, any other local regulatory authorities as required by countries and in accordance with ICH/GCP and applicable country regulations/guidelines.
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
Matching Summary
As a Site Specialist I at ICON, you will support investigator sites with key administrative and operational activities to help ensure clinical trials run smoothly, efficiently, and in compliance with applicable regulations.
Skills & Requirements
Must-have
ICON SOPs/WPs, ICH/GCP
country regulations/guidelines
clinical study start up
regulatory processes and submissions
read clinical protocols
manage multiple tasks simultaneously
Nice-to-have
foster an inclusive environment
drive innovation and excellence
support well-being and work life balance
Key Requirements
Bachelor’s Degree preferably in Life Sciences
+2 years’ experience
Knowledge of local and/or international regulatory processes
Ability to work independently
Excellent communication skills in English and Spanish