ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
The role involves monitoring clinical trial sites to ensure adherence to protocols, regulatory requirements, and GCP standards while supporting site staff and managing multiple projects.
ICON offers competitive salary and a range of benefits focused on well-being, work-life balance, and a diverse, inclusive culture.
Matching Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
Skills & Requirements
Must-have
Monitoring clinical trial sites
Good Clinical Practice (GCP) standards
Clinical trial software proficiency
West coast US location
60% travel availability
Oncology study monitoring experience
Nice-to-have
Cross-functional team collaboration
Training and guidance provision
Stakeholder management skills
Problem-solving skills
Inclusive work environment
Key Requirements
Advanced degree in life sciences, nursing, or medicine