Experienced Technical Writer and detailed Technical Editor with extensive academic and professional experience crafting procedures, policies, best practices, white papers, and other documents for a wide range of audiences. Familiarity with regulated healthcare and validated pharmaceutical environments, including knowledge of FDA (21 CFR Part 11, PDMA) and HIPAA guidelines. Extensive knowledge in the area of document design, including experience with usability testing and user-centered design techniques. Outstanding communicator and researcher capable of gathering, organizing, and effectively relaying complex technical information on a wide range of topics, and to a diverse array of target audiences.