Carol I. Matthews
Senior Director of Clinical Programming
United BioSource Corporation
Carol I. Matthews is Senior Director of Clinical Programming at United BioSource Corporation (UBC), where she mentors management-level programming staff. She develops, documents, and maintains a centralized macro library, and is responsible for the migration of SAS software. A SAS user since 1990, Carol is a frequent presenter at the Pharmaceutical Industry SAS Users Group (PharmaSUG).
The author also teaches the "SAS Programming Certificate for the Pharmaceutical Industry" course for Philadelphia University's continuing education program. The program addresses good programming practices, common clinical data sets, reporting with data _null, and SAS macros.
By This Author
Validating Clinical Trial Data Reporting with SAS®
This indispensable guide focuses on validating programs written to support the clinical trial process from after the data collection stage to generating reports and submitting data and output to the Food and Drug Administration (FDA). The authors provide practical examples and tips for avoiding errors in your output.
- Marie Gaudard is a consultant specializing in statistical training with the use of JMP. She is currently a statistical writer with the JMP documentation team
- Satish Garla is a former Analytical Consultant in Risk Practice at SAS.
- Sam Gardner is a Senior Research Scientist at Eli Lilly and Company where he is focusing on business analytics and using statistical modeling.