Douglas Kent is an Associate Director in Global Regulatory Affairs, specializing in Business Outcomes Delivery. With over twenty years of hands-on experience in Regulatory Information Management (RIM) at major pharmaceutical companies like GlaxoSmithKline and Johnson & Johnson, Douglas has developed a strong technical background and excellent leadership skills. They have a proven ability to handle high-pressure projects and are knowledgeable in various regulatory practices, including OPDP/APLB 2253 submissions and electronic publishing standards.
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