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 contact between investigational sites and sponsors, conducting site visits, ensuring compliance, and supporting patient safety and data quality.
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
Oncology clinical trial monitoring
ICH-GCP compliance
Site visit coordination
Clinical trial documentation management
Patient safety monitoring
Drug accountability oversight
Nice-to-have
Collaborative team player
Problem-solving skills
Clear communication
Willingness to travel up to 50%
Experience with CTMS and eTMF systems
Key Requirements
Bachelor’s degree in Life Sciences or equivalent
Qualified RN
2+ years on-site monitoring experience
Experience in oncology clinical trials
Eligible to work in United States without visa sponsorship
Work Rights
Eligible to work in United States without visa sponsorship