Site Specialist I

ICON plc

Multiple Locations
Site document collection and tracking
Clinical trial management systems
Site-related documentation filing
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.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.

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

  • Site document collection and tracking
  • Clinical trial management systems
  • Site-related documentation filing
  • Collaborate with project teams
  • Support investigator sites

Nice-to-have

  • Customer-focused approach
  • Inclusive and diverse culture
  • Work-life balance opportunities

Key Requirements

  • Bachelor's degree or equivalent experience
  • Excellent English and Portuguese
  • Initial experience in clinical research
  • Strong organizational skills
  • Good communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter