Stephanie Dubois PhD, RAC, CCRP

Dr. Dubois has more than 12 years' experience in product development and academic science. She has basic research experience in endocrinology and rheumatology in the areas of drug metabolizing enzymes, bone metabolism, bone physiology, phosphate and calcium homeostasis, and renal physiology. Since joining Cato Research, Dr. Dubois has gained experience in various aspects of product development and clinical research, including clinical and regulatory strategy development, clinical trial design and conduct, and scientific support. As a senior scientist, Dr. Dubois serves as project manager or clinical study manager and manages all aspects of her projects, including clinical trial conduct, overseeing the authors of clinical and regulatory documents, and managing project budgets and timelines. Her projects have involved pharmaceuticals, biologics, and medical devices in various therapeutic areas, including dermatology, gastroenterology, hematology, neurology, oncology, pulmonology, and rheumatology. She has participated in the preparation, writing, and revision of clinical documents, clinical study reports, integrated development plans, as well as various Health Canada and Food and Drug Administration meeting information packages and applications. Dr. Dubois has earned her Clinical Research Professional Certification from the Society of Clinical Research Associates and is Regulatory Affairs Certified by the Regulatory Affairs Professionals Society.


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