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Prepare for a Job in Clinical Trials Design and Management
Join us for a 90-minute informal info session about UCSC Extension’s certificate in Clinical Trials Design and Management, a program unparalleled in rigor and quality. We help professionals gain a solid and practical understanding of the entire clinical trials process—from drug and device development to monitoring—while providing you with a foundation in the scientific principles, regulations, and the ethics that are vitally important to the conduct of clinical research. This comprehensive curriculum and intense focus on best practices in the clinical trial process makes this certificate program an excellent choice for current professionals—clinical research associates and coordinators, clinical program managers and physicians, biomedical and research scientists, nurses, IRB members and administrators, and pharmacists—as well as those who are new to the field.
Presenter: Edward Rozhon
EDWARD ROZHON, Ph.D., chair of the Bioinformatics, Biotechnology, and Clinical Trials Design and Management programs, has had a long career in the biopharmaceutical industry as a contributor to the development of drugs to treat viral and autoimmune diseases, as well as several types of cancer. He has worked in both nonclinical and clinical areas of drug development, in the global pharmaceutical and biotech industry, in a contract research organization to support clinical research as well as in academia. He retired from Genentech in 2014 as a senior manager of clinical trials for autoimmune, infectious, and ophthalmologic diseases. On completing his doctorate at Indiana University, he pursued post-doctoral training in neurovirology at the University of Alabama School of Medicine and at Northwestern University School of Medicine and was subsequently appointed to a faculty position in microbiology and immunology. He has taught courses in drug development and virology at UCSC Extension since 2001.
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