Statistics in Clinical Trials

Oncology Clinical Trials

What, Who, When, Where, Why

Scope—Clinical Research focused on clinical trials in oncology

• Design, conduct of trials, relevant regulatory ethics and data management issues, barriers and challenges, and career development
• Introduction to other types of clinical research and adjuncts to therapeutic trials including biomarkers and correlative studies

Audience

• Interested fellows and faculty in a cancer-related division or department
• Including learners from med onc, hem onc, gyn onc, urologic oncology, ENT, pediatric oncology, surgical oncology, radiation oncology
• Oncology APPs

Format

• Synchronous learning: 7-8 sessions, zoom and video recorded for access anytime
• Asynchronous learning (ie: TRACS series, CITI training, LCCC training modules, etc)*
• Mentored learning (PRC, IRB, DSMC, protocol development)*

* possibly year 2-3

Please note that after registering for this course, you will receive a separate confirmation email for each class within the course. We apologize for the inconvenience of sending so many emails at once. Moving forward, you will receive reminder emails approximately one day and one hour prior to each individual class, but only for the pending class.

Statistics in Clinical Trials

J. Anastasia Ivanova, PhD

Professor
Department of Biostatistics
UNC Lineberger Comprehensive Cancer Center
UNC School of Medicine
University of North Carolina at Chapel Hill

Allison M. Deal

Biostatistician
UNC Lineberger Comprehensive Cancer Center
UNC School of Medicine
University of North Carolina at Chapel Hill

Register to Attend in Our Learning Portal