Ed Matthews is a biostatistician with 26 years’ experience in medical statistics, having worked on multiple clinical studies, in a wide cross-section of therapeutic areas, focused on oncology, and in all clinical phases (I to IV). He is practiced in working on a variety of study requirements, including SAPs, electronic Case Report Forms (eCRFs), Clinical Study Reports (CSRs), protocols, clinical summaries and ISS/ISE, both in the UK, Europe and globally. Ed also has many years’ experience of PK analysis, in guiding and training both Statisticians and non-Statisticians, and experience with data safety boards as both an attendee and chair.
Phase I Clinical Trial Designs: Bayesian Optimal Interval Design (BOIN)
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