Russ Neubauer Ph.D

Dr. Neubauer has over 35 years of experience in the areas of oncology, infectious diseases, women’s health, hematology, immunology, vaccines, virology, and toxicology. He has over 25 years’ experience in the pharmaceutical industry and has led productive teams of as many as 20 individuals. Dr. Neubauer has participated in the creation and implementation of product development strategies and had responsibility for the preparation and approval of documents and reports intended for submission to US and foreign regulatory agencies. These documents include product labels; NDA, BLA, and European dossier submissions; responses to questions from regulatory agencies; Corporate Direction Circulars; IND submissions; IND annual reports; clinical study reports; Investigator’s Brochures; preclinical research reports; and toxicology study reports. He has served on committees for national and regional scientific associations, authored 74 publications, 89 presentations, and 5 patents.

By effectively combining leadership, expertise, and knowledge of corporate and regulatory requirements Dr. Neubauer is able to achieve project goals. Communication and interpersonal skills, demonstrating initiative, flexibility, and innovation help him to effectively manage resources, programs, and projects for clients. He believes the best project results derive from the efforts of an interactive team and a desire for continuous improvement.

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