You will be monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
Job Summary
You will be monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
You will be collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.
Matching Summary
You will be monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Skills & Requirements
Must-have
monitoring clinical trial sites
ensure adherence to protocols
conduct site visits
collaborate with cross-functional teams
build relationships with site personnel
Nice-to-have
foster inclusive environment
drive innovation and excellence
support creativity and collaboration
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate
Proven ability to manage multiple sites
Working knowledge in monitoring complex, early Phase Oncology trials