Strategy and Statistics in Clinical Trials

A Non-Statisticians Guide to Thinking, Designing and Executing

Nonfiction, Health & Well Being, Medical, Medical Science, Pharmacology, Science & Nature, Mathematics, Statistics
Cover of the book Strategy and Statistics in Clinical Trials by Joseph Tal, Elsevier Science
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Author: Joseph Tal ISBN: 9780123869920
Publisher: Elsevier Science Publication: June 26, 2011
Imprint: Academic Press Language: English
Author: Joseph Tal
ISBN: 9780123869920
Publisher: Elsevier Science
Publication: June 26, 2011
Imprint: Academic Press
Language: English

Strategy and Statistics in Clinical Trials deals with the research processes and the role of statistics in these processes. The book offers real-life case studies and provides a practical, how to guide to biomedical R&D. It describes the statistical building blocks and concepts of clinical trials and promotes effective cooperation between statisticians and important other parties.

The discussion is organized around 15 chapters. After providing an overview of clinical development and statistics, the book explores questions when planning clinical trials, along with the attributes of medical products. It then explains how to set research objectives and goes on to consider statistical thinking, estimation, testing procedures, and statistical significance, explanation and prediction. The rest of the book focuses on exploratory and confirmatory clinical trials; hypothesis testing and multiplicity; elements of clinical trial design; choosing trial endpoints; and determination of sample size.

This book is for all individuals engaged in clinical research who are interested in a better understanding of statistics, including professional clinical researchers, professors, physicians, and researchers in laboratory. It will also be of interest to corporate and government laboratories, clinical research nurses, members of the allied health professions, and post-doctoral and graduate students.

  • Enables non-statisticians to better understand research processes and statistics' role in these processes
  • Offers real-life case studies and provides a practical, "how to" guide to biomedical R&D
  • Delineates the statistical building blocks and concepts of clinical trials
  • Promotes effective cooperation between statisticians and important other parties
View on Amazon View on AbeBooks View on Kobo View on B.Depository View on eBay View on Walmart

Strategy and Statistics in Clinical Trials deals with the research processes and the role of statistics in these processes. The book offers real-life case studies and provides a practical, how to guide to biomedical R&D. It describes the statistical building blocks and concepts of clinical trials and promotes effective cooperation between statisticians and important other parties.

The discussion is organized around 15 chapters. After providing an overview of clinical development and statistics, the book explores questions when planning clinical trials, along with the attributes of medical products. It then explains how to set research objectives and goes on to consider statistical thinking, estimation, testing procedures, and statistical significance, explanation and prediction. The rest of the book focuses on exploratory and confirmatory clinical trials; hypothesis testing and multiplicity; elements of clinical trial design; choosing trial endpoints; and determination of sample size.

This book is for all individuals engaged in clinical research who are interested in a better understanding of statistics, including professional clinical researchers, professors, physicians, and researchers in laboratory. It will also be of interest to corporate and government laboratories, clinical research nurses, members of the allied health professions, and post-doctoral and graduate students.

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