Director of Technology Assessment, Hospira Inc., U.S.
Mary Gardner, Director of Technology Assessment, Hospira Inc. Lake
Forest, Illinois. In her role at Hospira, Mary is focused on bringing in
new technology and product opportunities to support Hospira's inorganic
growth. She leads efforts for the identification & evaluation of these
external candidates. Mary's experience in the healthcare and biotech
industries includes positions in consulting, process & design
engineering and project management. Prior to joining Hospira she held
the position of Business Development Manager for the Lawson Health
Research Institute and London Health Sciences Centre, London, Ontario
where she was responsible for technology transfer & spin-off of
companies created from Innovations arising out of leading Canadian
teaching hospitals. She holds an MBA from McMaster University, Hamilton
and a BEngSc (Chemical & Biochemical) from the University of Western
Ontario, London.
Andy Hull
Vice President, Global Alliance Management, Takeda Global Research & Development Center, Inc., U.S.
Andy Hull, Vice President of Global Alliance Management at Takeda, oversees
the company's commercial and R&D partnerships. Hull is a 20 year veteran of
the pharmaceutical industry having held leadership positions at Abbott,
Immunex (acquired by Amgen) and TAP (now Takeda). His roles have included
VP of Specialty Therapeutics Marketing, Senior Vice President of Marketing
and Senior Vice President of Business Development and Strategic Product
Planning. This past January, Andy was elected Chairman of the Illinois
Biotechnology Industry Organization (iBIO) Board of Directors, a clear
demonstration of commitment to fostering growth of the life sciences sector
in Illinois.
Nancy Joseph-Ridge, M.D.
President, Takeda Global Research & Development Center, Inc., U.S.
Nancy Joseph-Ridge, M.D., is president of Takeda Global Research &
Development Center, Inc., U.S. In this capacity, Dr. Joseph-Ridge is
responsible for overseeing the organization's development activities. The
organization works to develop new product candidates, conduct post-marketing
clinical studies and identify and develop innovative lifecycle management
approaches for marketed drugs.
Previously, Dr. Joseph-Ridge worked at TAP Pharmaceutical Products Inc.,
where she was vice president of research and development. Having joined TAP
in 2002, she also served as therapeutic area head of Internal Medicine and
Rheumatology and department head for publications, medical writing and
clinical trial registries.
Before joining TAP, Dr. Joseph-Ridge gained experience in the cardiovascular
and arthritis therapeutic areas while working in drug safety and clinical
development at Searle, which has since become part of Pfizer.
She also brings extensive knowledge of internal medicine, rheumatology and
clinical trial work through her clinical and academic roles at the
University of Chicago and Rush-Presbyterian-St. Luke's Medical Center. At
the University of Chicago, Dr. Joseph-Ridge served as assistant professor of
medicine, director of the Lupus Clinic and medical director of the clinical
trials unit. In addition, she worked at Rush as clinical director of the
clinical research unit and the Lyme arthritis unit and was assistant
professor of medicine and assistant chairman of the department of Medicine
at Rush's medical school.
Dr. Joseph-Ridge earned her medical degree from the University of Illinois
at Chicago. She completed her internship and residency in internal medicine
at Rush Hospital, where she later became chief resident, and completed her
fellowship in Rheumatology at the University of Chicago. Dr. Joseph-Ridge is
board certified in both internal medicine and rheumatology.
Leonardo Sahelijo, M.D.
Director, Pharmacogenomics, Takeda Global Research & Development Center, Inc., U.S.
Dr Sahelijo studied chemistry at the Philipps University Marburg, Germany,
and received his medical degree from the University of Amsterdam, The
Netherlands. After several years of clinical practice in theNetherlands and
United Kingdom he joined the clinical drug development group of Knoll
AGLudwigshafen, Germany, in 1991. In 2001 he moved to the US to become
Abbott Laboratories global Medical Director Pharmacogenetics. Since 2007 he
is the Director Pharmacogenomics at Takeda Global Research and Development.