Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
Job Summary
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
ICON plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment driving innovation and excellence.
ICON offers a range of additional benefits designed to be competitive and focused on well-being and work life balance opportunities for you and your family.
Matching Summary
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
site performance assessment
timely data collection
site staff training
oncology study monitoring
Nice-to-have
foster inclusive environment
drive innovation and excellence
shape future of clinical development
well-being and work life balance
Key Requirements
Advanced degree in life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate