Mastering data management and analysis

Participants will gain a comprehensive understanding of best practices and strategies for collecting, managing, and analyzing clinical trial data to ensure accuracy, integrity, and compliance with regulatory standards. Through hands-on exercises and case studies, participants will learn how to leverage advanced tools and techniques to effectively manage and analyze clinical trial data, ultimately improving decision-making and enhancing the overall success of clinical trials.

• Introduction to Data Management in Clinical Trials
• Regulatory Requirements and Data Standards
• Data Collection Methods and Case Report Form (CRF) Design
• Data Entry, Cleaning, and Validation Processes
• Electronic Data Capture (EDC) Systems
• Data Quality Assurance and Quality Control
• Managing Missing Data and Handling Outliers
• Statistical Analysis Planning and Execution
• Interpretation and Presentation of Clinical Trial Results