: Deep background in regulatory medical writing and biotechnology product development, and a strong publication record in the peer-reviewed medical literature—an unusual combination of medical writing expertise, analytical skills, management experience, and medical knowledge. Experienced in all phases of drug, biologic, and medical device product development, with emphasis on clinical development. Manage medical writing groups, mentor and develop junior writers, and build medical writing infrastructure. Aims to strive excellence and prior job experiences to develop one's capabilities. Have an outstanding work rate and work ethic and is willing to discover and learn more in the field.