Senior Clinical Data Risk Analyst

Job Summary

To support clinical risk management initiatives, the full-time Senior Clinical Data Risk Analyst will lead the analysis of clinical trial data, identify risks, and implement mitigation strategies, working remotely or onsite across multiple US locations.

Key responsibilities:

• Conducting quality control and oversight activities within the Central Monitoring team
• Leading evaluations of clinical trial data to identify potential risks and trends affecting study outcomes
• Collaborating with cross-functional teams to develop and implement risk mitigation strategies to enhance data quality and integrity

Required qualifications:

• 5+ years of experience in clinical data analysis or risk management in a clinical research organization or pharmaceutical company
• Proficiency in statistical software and risk assessment methodologies
• Knowledge of at least one Clinical Data Management System (e.g., Medidata RAVE, InForm, Veeva)
• Bachelor's degree or local equivalent in life sciences or a related field preferred
• Ability to manage multiple studies simultaneously while adapting to changing priorities