Richann Watson
Independent statistical programmer and CDISC consultant
Richann Watson is an independent statistical programmer and CDISC consultant based in Ohio. She has been using SAS since 1996 with most of her experience being in the life sciences industry. She specializes in analyzing clinical trial data and implementing CDISC standards. Additionally, she is a member of the CDISC ADaM team and various sub-teams.
Richann loves to code and is an active participant and leader in the SAS User Group community. She has presented numerous papers, posters, and training seminars at SAS Global Forum, PharmaSUG, and various regional and local SAS user group meetings. Richann holds a bachelor’s degree in mathematics and computer science from Northern Kentucky University and master’s degree in statistics from Miami University.
By This Author
SAS® Graphics for Clinical Trials by Example
By Kriss Harris and Richann Watson
Using real-world examples, this book shows programmers how to create clinical graphs in SAS. The book demonstrates step-by-step how to create both simple and complex graphs using Graph Template Language (GTL) and statistical graphics procedures, including the SGPLOT and SGPANEL procedures.
*Our books are also available in print and e-book formats
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Book Reviews
"The book is a highly concentrated exposition of how graphics can be used to illuminate the meaning of clinical trials data. As such, it must be sipped, not gulped. The authors have put a tremendous amount of thought into the content. Every part of the book is valuable and must be digested slowly and carefully. "
Dr. Jim Sattler, President
Satmari Software Systems, Inc.
"There are examples for graphical representation of adverse events, which are not commonly included in Clinical Study Reports in the United States, but are used more often in Europe. Armed with this book, programmers can approach statistical graphics with confidence! This book is a MUST-HAVE."
Alice Cheng
Featured Authors
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Todd Case has been working in the pharmaceutical industry as a statistical programmer for over 20 years. He completed his MS in Epidemiology from Columbia University and has worked at Forest Laboratories (now Allergan), Genentech, Bristol-Myers Squibb, and Biogen. He currently works at Vertex Pharmaceuticals.
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Terisa Roberts is a director and Global Solution lead for Risk Modeling and Decisioning at SAS. She has extensive experience in quantitative risk management, regulatory compliance, and model governance and validation. She has worked in financial services, telecommunications, government, energy, and retail sectors.
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Robert N. Rodriguez retired from SAS in 2018 after serving as a senior director in research and development. Bob received a PhD in statistics from the University of North Carolina at Chapel Hill and was a research statistician at General Motors Research Laboratories before joining SAS.
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Ron Klimberg, PhD, is a professor at the Haub School of Business at Saint Joseph's University in Philadelphia, PA.