Rachel Bleich, CBMC
This course will offer best practices when conducting clinical trials using FDA approved and non-approved drugs or substances (including botanicals and biologics). It will cover the IND process and the regulatory obligations of the sponsor- investigator once an IND is filed with the FDA.
Karin Leiderman, PhD, Assistant Professor, Department of Applied Mathematics, University of California, Merced
Anna Marie Pyle, Ph.D. Yale University
150 Dubose Home Ln, Chapel Hill, NC
Join us on Friday, October 30, 2015 for the 7th Annual Coping with Cancer Symposium, being held at the Rizzo Center in Chapel Hill. This year's event, titled "Identification and Management of Late Effects of Cancer Treatment" will feature multidisciplinary presentations of the latest advances in acute, long-term, chronic and late effects of treatment, including psychosocial consequences and surveillance for recurrence within the cancer survivorship population.
This training will cover the various ways the electronic medical record can be used to facilitate research recruitment including use of the Carolina Data Warehouse (CDW) and i2b2. As UNC Healthcare has expanded to include affiliate hospitals around the state, helping study coordinators, researchers and recruiters understand the sensitivities involved in approaching patients about research at all the healthcare system hospitals is a priority. This training will provide research personnel with tips, tools and resources to aid in research recruitment and best practices for approaching potential research participants.
Ryan Potts, PhD, Assistant Professor, Department of Physiology, Pharmacology and Biochemistry, UT Southwestern Medical Center
Sharon Hilgen-Willis, Integral Molecular
Symposium Sponsored by the Department of Pharmacology and the Curriculum in Bioinformatics and Computational Biology
David Muddiman, PhD, Distinguished Professor, Department of Chemistry, NC State University