The overall goal of this master's degree program is to prepare competent individuals to
work in the biopharmaceutical industries, regulatory agencies, contract research organizations, or academia, with the primary objective of assisting with the execution
and reporting of clinical drug and device trials commensurate with clinical, legal, ethical,
and regulatory guidelines. This is performed through a competency-based framework
covering the following domains: Scientific Concepts and Research Design, Ethical and Participant Safety Considerations, Medicine Development and Regulation, Clinical Trial Operations, Study and Site Management, Data Management and Informatics, Leadership and Professionalism, and Communication and Teamwork.
Health Informatics 
