Master of Science - Clinical Trials and Regulatory Affairs

The Master of Science (MSc) degree in Clinical Trials and Regulatory Affairs is a forward-thinking program tailored to meet the healthcare research community, government, and industry demands. It equips students with the knowledge and skills to design, conduct, manage, and evaluate clinical trials across various healthcare environments.

Clinical trials are crucial research studies involving human participants to assess the safety and efficacy of therapeutic interventions. This MSc program offers graduates in-depth knowledge and practical expertise, preparing them for success in clinical trials and regulatory affairs. Students gain hands-on experience through collaborations with leading organizations in the field. For those without prior experience, the program includes a four-month practicum, providing placements at research institutes, government agencies such as Health Canada, pharmaceutical companies, and contract research organizations.

The program is delivered through a flexible hybrid model that combines in-person and online courses. This approach accommodates students from various locations, especially outside Ottawa, reducing the need for extended relocation. The curriculum covers various topics, including the fundamentals of clinical trials, regulatory requirements, data management, patient safety, management, communication, and ethical considerations.

Graduates will be well-prepared for clinical research and regulatory affairs careers, with the skills to navigate the complexities of clinical trials and regulatory processes. This MSc program offers a unique educational opportunity, enabling students to develop critical competencies and engage with industry leaders, ultimately contributing to healthcare innovation.