Join us on May 26, 2021 from 2-3:30pm ET for a NAACCR Talk "Secondary Release of Cancer Registry Data"
Registration is free at:
The purpose of this webinar is to discuss how registries can better understand and support the NCI data sharing requirements for researchers, which for some registries currently pose significant barriers. A significant and related topic, demonstration of data sharing methodologies, will be presented in the future.
Setting the Stage: Conflicts between NIH data sharing requirements for researchers and registry secondary data release policies--how to improve
Dennis Deapen, DrPH, MPH
Past Director, Los Angeles Cancer Surveillance Program
NIH Policies on Data and Resource Sharing
Nonye Harvey, DrPH
Health Science Policy Analyst, National Institute of Health
Julia Slutsman, PhD
Director Genomic Data Sharing Implementation, National Institute of Health
Strength in Numbers: Cancer Research in the NCI Cohort Consortium
A. Heather Eliassen, Sc.D.
Associate Professor, Harvard and Brigham & Women's Hospital
The PLCO Cancer Screening Trial: Navigating restrictions to share registry-linked data with the cancer research community
Eric Miller, PhD
Epidemiologist, National Cancer Institute
Envisioning the Way Forward...Together
Castine Clerkin, MPH
Program Manager Virtual Pooled Registry, NAACCR
Angela Martin, CTR
Training Specialist/Project Coordinator
Phone: 217-698-0800 ext. 9