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The Master of Science (MSc) in Clinical Trials and Regulatory Affairs is an innovative program designed to address the needs of healthcare research, government agencies, and industry sectors. This program provides comprehensive training in designing, overseeing, managing, and analyzing clinical trials in diverse healthcare settings. As essential investigations involving human subjects, clinical trials evaluate the effectiveness and safety of medical treatments. The MSc curriculum delivers specialized knowledge and practical competencies, enabling graduates to excel in clinical research and regulatory compliance. Through partnerships with top-tier institutions, students acquire real-world experience. For newcomers to the field, the program incorporates a four-month internship with opportunities at research centers, regulatory bodies like Health Canada, drug manufacturers, and clinical research firms.