ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence.
As a Site Specialist II, you will independently manage site support activities, coordinate documentation, act as a liaison for site staff, and contribute to process improvements.
ICON offers competitive salary and 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 plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence.
Skills & Requirements
Must-have
Site-level document management
Clinical trial process knowledge
GCP compliance understanding
Clinical trial management tools
Site workflow optimization
Cross-functional team collaboration
Nice-to-have
Proactive service mindset
Strong organizational skills
Problem-solving abilities
Excellent communication skills
Experience mentoring junior colleagues
Key Requirements
Bachelor’s degree or equivalent clinical research experience
Experience in site support or clinical administration
Understanding of clinical trial documentation requirements