ICON is seeking an Analytical Monitor for a remote position in Mexico City to support clinical trial oversight through data analytics, risk identification, and reporting. The role involves analyzing site and subject-level data across multiple systems to identify trends and quality issues, collaborating with cross-functional teams to support informed decision-making.
Responsibilities
Conduct analytical monitoring across assigned clinical trials to identify trends and data quality issues
Perform regular site and subject-level reviews for proactive issue detection
Access and analyze data from multiple systems and databases to support decision-making
Collaborate with Site Managers and Central Monitoring on risk management and site prioritization




Communicate with stakeholders following escalation pathways while maintaining regulatory compliance
Requirements
Bachelor's degree in Health Sciences, Data Sciences, or related field
2+ years pharmaceutical, CRO, biotech, or related industry experience
Strong data analysis and interpretation skills in clinical research
Working knowledge of ICH-GCP and regulatory frameworks
Experience with data collection, analysis, and reporting technology platforms
Strong organizational skills managing multiple priorities
Fluent English verbal and written communication

📌 Analytical Monitor (Xico)
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📍 Xico