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New hire will head division devoted to clinical and regulatory staffing.
Aptiv Solutions has appointed Patricia Monteforte as president of Trio Clinical Resourcing, a subsidiary devoted to clinical and regulatory staffing. Monteforte will leverage more than 25 years in the pharmaceutical industry and success leading clinical research organizations to assemble teams of qualified clinical and regulatory professionals to deliver flexible resourcing solutions to meet the current and future challenges in the pharmaceutical and medical device industry.
Most recently, Monteforte served as INC Research LLC’s executive vice president of clinical development and general manger. During her tenure at INC, she supervised the operations of 500 employees across numerous specialties, including infectious diseases, vaccines, immunology/inflammation, respiratory, gastroenterology, dermatology, pediatrics, late phase trials, cardiovascular, endocrinology, ophthalmology and oncology. Before joining INC Research in 2006, Monteforte founded and served as president and CEO of the Pharmaceutical Resource Corporation, which grew into a full-service contract research organization for pediatrics and peri/post-approval studies. She also founded and led Pharmaceutical Staffing Solutions, which provided both permanent and flexible staffing solutions to many of the 10 largest pharmaceutical companies.
Monteforte holds a Bachelors of Arts degree in biology from Franklin and Marshall College. She is a member of the Drug Information Association and has served on the Advisory Council for the Center for Women’s Business Research. She has received the Pennsylvania Best 50 Women in Business Award and was one of 14 women honored in the national Salute to Women’s Business Enterprises.
Aptiv Solutions is a global development services company that is focused on enhancing clinical trial decision-making, efficiency and productivity in the pharmaceutical, biotech and medical device markets. The company offers clients a portfolio of services including adaptive clinical trials, translational research services, regulatory services, pharmacovigilance, clinical staffing and the operational support of a global clinical research organization. The firm employs more than 850 professionals in North America, Eastern and Western Europe, Israel and Japan.
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