ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
The role involves serving as the primary point of contact between investigational sites and the sponsor, ensuring compliance, monitoring patient safety, and supporting site staff training.
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 fostering an inclusive environment driving innovation and excellence.
Skills & Requirements
Must-have
On-site monitoring experience
ICH-GCP compliance
Clinical trial management systems
Oncology clinical trials
Site visit coordination
Patient safety monitoring
Nice-to-have
Collaborative team player
Problem-solving skills
Clear communication
Cross-functional collaboration
Travel flexibility
Key Requirements
Bachelor’s degree in Life Sciences or equivalent
Qualified RN
2+ years on-site monitoring experience
Experience in oncology trials
Eligible to work in United States without visa sponsorship
Willingness to travel up to 50%
Work Rights
Eligible to work in United States without visa sponsorship