ICON seeks an Advanced Analytical Monitor for remote work in Mexico City to conduct data-driven risk identification across mid to high-complexity clinical trials. The role involves analyzing site and subject-level data, collaborating with cross-functional teams, and mentoring junior colleagues to support trial integrity and operational efficiency.
Responsibilities
Perform analytical monitoring to identify site and subject-level risks, trends, and data quality issues early
Conduct regular data reviews at site and subject levels to detect warning signals and prevent recurrence
Access and analyze data from multiple systems and databases to support informed decision-making
Collaborate with Site Managers and Central Monitoring to influence risk management prioritization




Mentor junior Analytical Monitors and provide training to support team capability development
Requirements
Bachelor's degree in Health Sciences, Data Sciences, or related field; Master's preferred
4+ years experience in pharmaceutical, biotech, or CRO industry
Strong understanding of clinical trial operations and data flow in clinical research
Demonstrated data analysis experience in clinical research with statistical knowledge
Project, issue, and risk management experience with critical thinking ability
Proficiency with clinical data collection, analysis, and reporting technology platforms
Fluent English communication skills, both verbal and written

📌 Analytical Monitor (Xico)
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📍 Xico