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| Joseph S. Anderson, Principal Associate, focuses on the issues surrounding technology choice and implementation, with a special expertise in technology implementation, the financial analysis of clinical research software adoption and process change. Mr. Anderson also leads our drug safety operations optimization practice. Mr. Anderson has over 15 years experience in the pharmaceutical industry, including nine years consulting to European and U.S. pharmaceutical companies while living in Germany. He joined Waife & Associates in 1998.
Mr. Anderson has done groundbreaking work in the area of clinical research metrics. He has developed sustainable metrics programs for various clients that measure both costs and productivity in the conduct of clinical trials. He has also developed cost/benefit and ROI models for enterprise software acquisition at multinational biopharmas.
Previously Mr. Anderson was a Project Manager at Technilogix, Inc., a second generation EDC provider. Before that, he spent five years with Eli Lilly and Company, designing various clinical data systems to support all aspects of the clinical trial process. In addition, Mr. Anderson worked at the Lilly German affiliate, where he was European project manager for the design and implementation of a worldwide electronic data capture system.
Mr. Anderson has a B.S. in computer science and mathematics from Grand Valley State University in Allendale, Michigan. He is fluent in German and staffs our Research Triangle Park, NC office. Mr. Anderson has contributed to various industry publications and is a frequent presenter at industry meetings.
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