{"id":5082,"date":"2024-07-26T15:52:37","date_gmt":"2024-07-26T19:52:37","guid":{"rendered":"https:\/\/carleton.ca\/healthsciences\/?page_id=5082"},"modified":"2026-05-22T10:31:15","modified_gmt":"2026-05-22T14:31:15","slug":"professional-m-sc-in-clinical-trials-and-regulatory-affairs","status":"publish","type":"page","link":"https:\/\/carleton.ca\/healthsciences\/health-sciences\/graduate\/professional-m-sc-in-clinical-trials-and-regulatory-affairs\/","title":{"rendered":"Professional MSc in Clinical Trials and Regulatory Affairs"},"content":{"rendered":"\n
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\n Professional MSc in Clinical Trials and Regulatory Affairs\n <\/h1>\n \n \n <\/header>\n\n <\/div>\n\n <\/div>\n\n <\/div>\n<\/section>\n\n\n\n

Discover the forefront of clinical trials and regulatory affairs with Carleton University\u2019s Master of Science (MSc) in Clinical Trials and Regulatory Affairs. This primarily online course-based program<\/strong> 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.<\/p>\n\n\n\n

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.<\/p>\n\n\n\n

For full-time students, the MSc program is completed over 16 months and consists of three (3) consecutive study terms<\/strong> and a four (4) month practicum<\/strong> consisting of a placement at research institutes, government agencies, pharmaceutical companies, and contract research organizations (CRO). Students with at least two (2) years of relevant experience<\/strong> in clinical trials and regulatory affairs may be exempted from the practicum and be eligible to complete the course-only pathway<\/strong> in 12 months.<\/p>\n\n\n\n

For part-time students, the MSc program is completed over 28 months and consists of six (6) consecutive study terms<\/strong> and a four (4) month practicum<\/strong> consisting of a placement at research institutes, government agencies, pharmaceutical companies, and contract research organizations (CRO). Students with at least two (2) years of relevant experience<\/strong> in clinical trials and regulatory affairs may be exempted from the practicum and be eligible to complete the course-only pathway<\/strong> in 24 months.<\/p>\n\n\n\n

Why choose Carleton’s MSc in Clinical Trials and Regulatory Affairs?<\/h2>\n\n\n\n