Lisa Fine
Assistant Manager of Clinical Programming, United BioSource Corporation
Lisa Fine is an Assistant Manager of Clinical Programming at United BioSource Corporation. She has more than 15 years of experience in applied SAS programming with a focus on data verification and reporting in Pharmaceutical Research and Marketing. Lisa’s expertise with SAS encompasses a significant amount of DATA step processing and using a variety of procedures, including PROC REPORT, PROC SQL, PROC FREQ, PROC MEANS, and PROC UNIVARIATE. She graduated from Loyola University in Chicago with an MA in Research Methodology from the School of Counseling and Education. Lisa is a certified SAS Base Programmer for SAS 9, SAS Advanced Programmer for SAS 9, and SAS Certified Clinical Trials Programmer Using SAS 9.
By This Author
PROC REPORT by Example: Techniques for Building Professional Reports Using SAS®
By Lisa Fine
Featured Authors
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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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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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Ron Klimberg, PhD, is a professor at the Haub School of Business at Saint Joseph's University in Philadelphia, PA.
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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.