Last updated on 2025-04-25
Program Overview
The Professional Master of Science (MSc) degree in Clinical Trials and Regulatory Affairs is a forward-thinking program tailored to meet the needs of the healthcare research community, government, and industry. This program equips students with essential knowledge and skills to design, conduct, manage, and evaluate clinical trials across various healthcare settings. It is particularly suitable for recent graduates in health sciences, life sciences, or related fields, as well as mid-career professionals looking to advance their careers or transition into clinical trials or regulatory affairs.
With the increasing globalization of regulatory requirements and innovative approaches like decentralized clinical trials, this program prepares students for the future of healthcare research. Graduates will gain practical expertise and in-depth knowledge, positioning them for successful careers in clinical trials and regulatory affairs.
Program Structure
The MSc program in Clinical Trials and Regulatory Affairs is structured to accommodate both full-time and part-time students:
- Program Length:
- Full-Time: 2 years
- Part-Time: 3 years
- Entry Terms: Fall
- Application Deadline: March 1 for both domestic and international candidates
- Pathway Options: Coursework, Practicum
The program is delivered through a flexible hybrid model, combining in-person and online courses, which allows working professionals to balance their studies with their current roles. Students will also benefit from a four-month practicum, providing hands-on experience with research institutes, government agencies, pharmaceutical companies, and contract research organizations.
Featured Experiences
- Hands-on experience through collaborations with leading organizations in the field.
- Four-month practicum placements with various research and regulatory bodies.
- Flexible course schedules that accommodate working professionals.
- Engagement with industry leaders to build critical competencies.
Career Options
Graduates of the MSc in Clinical Trials and Regulatory Affairs can pursue various career paths in Canada, including:
- Clinical Research Associate: Responsible for monitoring clinical trials and ensuring compliance with regulatory standards.
- Regulatory Affairs Specialist: Works to ensure that products meet all regulations and standards before they can be marketed.
- Clinical Trials Manager: Oversees the planning and execution of clinical trials, managing teams and budgets.
- Data Manager: Focuses on the collection, management, and analysis of clinical trial data.
- Quality Assurance Officer: Ensures that clinical trials are conducted according to established protocols and regulatory requirements.
DISCLAIMER: The information above is subject to change. For the latest updates, please contact LOA Portal's advisors.
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