The Master of Science in Clinical Trial Management will harnesses the depth and breadth of Regulatory and Quality Science course content and focuses on foundational topics related to the successful management of clinical trials, including regulatory compliance, scientific writing, marketing, data management, project management and quality assurance. The field of clinical research is focused on developing cost-effective ways to treat disease and increase quality of life through successful development and launch of new biologics, devices and pharmaceuticals, and by incorporating the science of genomics or personalized genetic prescribing. Employment settings include pharmaceutical, biotechnology, medical device companies, contract research, hospitals, educational institutions and independent contractors.
The program requires a minimum of 32 units.
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