Discover the forefront of clinical trials and regulatory affairs with Carleton University’s Master of Science (MSc) in Clinical Trials and Regulatory Affairs. This course-based program has been developed to provide healthcare professionals and science graduates with an opportunity to enhance their clinical and research skills by engaging with a community of experts dedicated to advancing the field of clinical trials. Our faculty includes leading researchers, experienced clinicians, and regulatory professionals who are committed to providing students with unparalleled insights and hands-on experience.
As the first program of its kind in Ontario, students will delve into the scientific, methodological, and regulatory dimensions of clinical trials. From the intricacies of early-phase studies to the complexities of late-stage interventions, students will gain a comprehensive understanding of trial design, conduct, analysis, and reporting. Students will also develop vital communication skills through both individual and collaborative activities, preparing them to effectively navigate the regulatory landscape and lead in the industry.
The MSc program consists of three (3) consecutive study terms and a four (4) month practicum consisting of a placement at research institutes, government agencies, pharmaceutical companies, and contract research organizations (CRO) The program is completed over 16 months of full-time studies or 28 months of part-time studies.
Note: Students with at least two (2) years of relevant experience in clinical trials and regulatory affairs may be exempted from the practicum and be eligible to complete the course-only pathway.
Why choose Carleton’s MSc in Clinical Trials and Regulatory Affairs?
- Expert faculty: Learn from the best. Our program features a diverse team of experts who bring cutting-edge research and industry experience right into the classroom.
- Flexible hybrid model: With online lectures, students can complete the program remotely providing an opportunity to form international collaborations.
- The program can be completed in 16 months (full-time) or 28 months (part-time) to accommodate working professionals and promote career advancement while pursuing studies.
- Comprehensive curriculum: Gain in-depth knowledge of all phases of clinical trials, from initial concept through to final analysis and regulatory reporting. Understand the full spectrum of clinical trials – from simple intervention to complex multi-phase studies.
- Hands-on experience: Develop practical skills through interactive coursework and real-world case studies. Enhance your ability to communicate effectively in both individual and group settings.
- Career advancement: Position yourself at the forefront of the industry with a degree that opens doors to high-impact roles in clinical trials and regulatory affairs.