Clinical Data Risk Management Specialist

hace 2 semanas


Ciudad de México, Ciudad de México ICON Clinical Research A tiempo completo
Role Overview

This position is a critical part of our Central Monitoring team, responsible for ensuring the quality and integrity of clinical data. The ideal candidate will have strong analytical skills, proficiency in statistical software, and experience with clinical data management systems.

Key Responsibilities:

  • Signal tracking, system user support, and communication of trends to internal and external stakeholders
  • Conducting QC and oversight activities within the Central Monitoring team
  • Coordinating Central Monitoring sub-teams working with Sponsor specific processes
  • Contributing to team development
  • Leading risk assessments on clinical trial data to identify, evaluate, and mitigate potential risks
  • Developing and implementing risk management frameworks and protocols in alignment with regulatory standards
  • Collaborating with stakeholders to ensure effective communication of risk findings and recommendations
  • Monitoring data quality and compliance throughout the trial lifecycle, reporting on risk status and action plans
  • Providing training and guidance to teams on best practices for data risk management
About ICON

At ICON, we pride ourselves on being a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment that drives innovation and excellence, and we welcome talented individuals to join our mission to shape the future of clinical development.



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