Steven D. Reich, MD
Physician with over 50 years of drug research experience. Participated as an academically-based investigator for Phase I-III trials and designed and managed Phase I-IV trials for industrial sponsors. Extensive experience with computerized database management, including programming. Knowledge of pharmacokinetics, mathematical modeling, and biostatistics. Managerial experience includes directing multi-national medical research groups within pharmaceutical and biotechnology companies and a contract research organization. Headed the clinical research programs leading to five US, one Canadian, and two European (by centralized procedure) drug approvals.
Currently a semiretired, independent, clinical research and development consultant to pharmaceutical and biotechnology companies in the areas of strategic design of clinical programs and operational support of clinical trials. Specialties include clinical operational plans, protocol development, report and standard operating procedures writing, and medical monitoring.