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Dr. Johnson has nearly 30 years of experience with biostatistics in the pharmaceutical industry, including more than 20 years as a Statistical Consultant, advising clients on both statistical and regulatory aspects of clinical development programs. She previously spent 8 years at the FDA as a group leader and statistical reviewer in the Division of Biometrics. At PharmaNet, Dr. Johnson has managed statistical analysis and programming activities for clinical trials in numerous successful NDA/PLA submissions. She has developed statistical analysis plans for studies in most therapeutic areas as well as studies for devices and combination products. Dr. Johnson has authored dozens of publications and presentation for major journals and conferences. | 