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.
This is a highly collaborative, analytical role contributing to the overall quality, safety, and operational success of multiple clinical studies across global programmes.
ICON offers a range of 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 within clinical research
Clinical trial process knowledge
Risk identification and management
Cross-functional collaboration
Use of multiple data systems and reporting tools
Regulatory compliance adherence
Nice-to-have
Strong organisational skills
Excellent communication skills
Patient-centric decision support
Inclusive and diverse work culture
Key Requirements
Bachelor’s degree in Health Sciences or Data Sciences
2+ years experience in Pharmaceutical, CRO, or Biotech
Working knowledge of ICH-GCP and regulatory frameworks
Excellent verbal and written English communication