I am a Ph.D. Statistical and Process Consultant with more than 40 years of successful clinical and non-clinical drug development experience in eleven therapeutic areas with twelve NDAs.

My therapeutic area experience includes cardiovascular diseases, gastrointestinal disorders, infectious diseases, oncology, ophthalmology, pulmonary diseases, sleep disorders, vaccines, diagnostic agents, tuberculin diagnostic tests, medical devices and hospital products.

I developed my technical and management skills working at line and senior management positions in American and European multinational pharmaceutical companies with worldwide responsibility for Statistics, Data and Document Management, and Medical Systems. Consulting with top-tier companies in the pharmaceutical and information technology industries further enhanced the breadth and depth of my knowledge and experience, and has given me a wealth of practical and valuable insight into the discovery and development of biopharmaceutical/biotechnology products.

I have excellent technical knowledge and interpersonal skills. I make use of innovative, sound, and pragmatic approaches for effective staging and execution of development projects and clinical trials through optimal deployment of internal and external resources for faster development, approval, and transition of new drugs to marketing.

Whether your organization needs strategic consulting services or the managerial expertise required to take an important project from ground zero to fully operational status, I look forward to speaking with you about how I may be of service.