ICON is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment to shape the future of clinical development
Job Summary
ICON is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment to shape the future of clinical development.
The Site Specialist I will support investigator sites with administrative and operational activities to ensure clinical trials run smoothly, efficiently, and in compliance.
ICON offers competitive salary, a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.
Matching Summary
ICON is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment to shape the future of clinical development.
Skills & Requirements
Must-have
Collect and review essential site documents
Maintain accurate site information
Assist with site communications
Prepare materials for site visits
File site-related documentation
Resolve basic site queries
Nice-to-have
Foster an inclusive environment
Drive innovation and excellence
Customer-focused approach
Willingness to learn GCP principles
Key Requirements
Bachelor's degree or equivalent experience
Excellent English and Portuguese skills
Initial experience in clinical research or regulated environment preferred
Strong organizational skills and attention to detail