As an Analytical Monitor at ICON, you will play a crucial role in supporting clinical trial oversight through targeted data analytics, early risk identification, and the delivery of high-quality insights that empower Site Managers to make informed, patient-centric decisions
Job Summary
As an Analytical Monitor at ICON, you will play a crucial role in supporting clinical trial oversight through targeted data analytics, early risk identification, and the delivery of high-quality insights that empower Site Managers to make informed, patient-centric decisions.
Conducting analytical monitoring activities across assigned clinical trials to identify early trends, data quality issues, and potential risks at the site and subject level.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
Matching Summary
As an Analytical Monitor at ICON, you will play a crucial role in supporting clinical trial oversight through targeted data analytics, early risk identification, and the delivery of high-quality insights that empower Site Managers to make informed, patient-centric decisions.
Skills & Requirements
Must-have
data analysis and interpretation
clinical trial processes
ICH-GCP and regulatory frameworks
technology platforms and systems
cross-functional team collaboration
Nice-to-have
foster an inclusive environment
patient-centric decisions
work life balance opportunities
Key Requirements
2+ years of experience
Bachelor's degree in Health Sciences, Data Sciences or related field