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Principles and Practice of Clinical Trial Medicine
Ebook Free Principles and Practice of Clinical Trial Medicine
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About the Author
Richard Chin is the CEO of Institute for OneWorld Health, the first U.S. nonprofit pharmaceutical company and Associate Professor at UCSF School of Medicine. OneWorld Health develops affordable drugs for neglected patients in the developing world. Dr. Chin has extensive expertise in drug development, including over 45 INDs and almost a dozen drug registrations. His previous roles include CEO of a NASDAQ listed company, Senior Vice President of Global Development at Elan, and Head of Clinical Research for the Biotherapeutics Unit at Genentech. He was named by Businessweek in 2006 as one of the youngest 99 public company CEOs in the United States. Dr. Chin earned an M.D. from Harvard and the equivalent of a J.D. from Oxford, where he studied as a Rhodes Scholar.Dr. Lee is currently an Assistant Professor of Medicine and Biomedical Informatics at the University of Pittsburgh. He is also Core Faculty in the Section for Decision Sciences and Clinical Systems Modeling, the Center for Research in Health Care, and the RAND-University of Pittsburgh Health Institute. He is a Co-Investigator for the National Institutes of Health (NIH) Modeling of Infectious Diseases Agent Study (MIDAS) research and informatics network. His previous positions include serving as Senior Manager at Quintiles Transnational, working in biotechnology equity research at Montgomery Securities, and co-founding Integrigen, a biotechnology company. His consulting experience includes a large variety of clients, ranging from large and small pharmaceutical, biotechnology, and medical device companies.Dr. Lee has authored three books, as well as numerous research publications, review articles, and book chapters. Dr. Lee received his B.A. from Harvard University, M.D. from Harvard Medical School, and M.B.A. from the Stanford Graduate School of Business. He is board-certified in Internal Medicine, having completed his residency training at the University of California, San Diego.
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Product details
Hardcover: 560 pages
Publisher: Academic Press; 1 edition (July 2, 2008)
Language: English
ISBN-10: 0123736951
ISBN-13: 978-0123736956
Product Dimensions:
8.5 x 1.2 x 11 inches
Shipping Weight: 3.4 pounds (View shipping rates and policies)
Average Customer Review:
5.0 out of 5 stars
4 customer reviews
Amazon Best Sellers Rank:
#2,206,470 in Books (See Top 100 in Books)
As a newcomer to the pharma industry, this text is a must have to learn about clinical trials medicine through its early stages of development to advanced standards of clincal trial methodology. The text is easy to read and clearly guides the reader to understand all clinical trial components and processes. Perfect for students and industry persons alike, I highly recommend this book if you need to gain a thorough understanding of clinical trials research, from the basics of definition through comprehensive clinical trial analysis.
Best book I've seen to clearly distinguish terminology that is often mixed, as an instance, endpoints (outcome measures) and variables.......they are not one and the same! Must have in my library.
This is a really well written, comprehensive book. It covers just about anything you'd want to know about clinical studies. It will teach you a lot even if you've been doing clinical research for a while, it's very sophisticated. But not too many equations, although it has a few. You will probably find it very accessible even if you're new to clinical research.
I read this book because I was impressed by another book, Global Clinical Trials, which was edited by one of the authors.This is a pretty nice book that does a great job of covering a very wide range of fundamental topics that anyone doing clinical trials ought to know. It would have been great to have had this book when I started in industry.
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