The Professional Master of Science (MSc) degree in Clinical Trials and Regulatory Affairs is a forward-thinking program designed to address the demands of the healthcare research community, government, and industry. It equips students with the knowledge and skills to design, conduct, manage, and evaluate clinical trials across diverse healthcare settings. This program is ideal for recent graduates in health sciences, life sciences, or related fields, as well as mid-career professionals seeking career advancement or transitioning into clinical trials or regulatory affairs. It also caters to professionals in adjacent fields, such as engineering, nursing or laboratory science, who wish to expand their expertise and advance their careers.

Clinical trials are essential research studies involving human participants to assess the safety and efficacy of therapeutic interventions. With the increasing globalization of regulatory requirements and the rise of innovative approaches such as decentralized clinical trials, this program is designed to prepare students for the future of healthcare research. It delivers in-depth knowledge and practical expertise, preparing graduates for successful clinical trials and regulatory affairs careers. Students benefit from hands-on experience through collaborations with leading organizations in the field. For those without prior experience, the program includes a four-month practicum, offering placements with 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. It accommodates the needs of working professionals by offering flexible course schedules that balance in-person and online learning. Students can advance their careers without disrupting their current roles. The curriculum covers multiple topics, including the fundamentals of clinical trials, regulatory requirements, data management, patient safety, management and communication skills, and ethical considerations.

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

Important Information:

  • The courses-only pathway is available exclusively to candidates with at least two years of relevant professional experience;
  • Domestic candidates are strongly encouraged to submit their applications before March 1 to ensure consideration for admission to the Fall term. Applications may only be considered after March 1 if space remains in the program;
  • International candidates must submit complete applications by March 1.

Program Information

Length: Full-Time 2 years, Part-Time 3 years

Entry Terms: Fall

Fall Application Deadline: March 1

Domestic candidates are strongly encouraged to submit their applications before March 1 to ensure consideration for admission to the Fall term. Applications may only be considered after March 1 if space remains in the program.
International candidates must submit complete applications by March 1.

More Deadline Information »

Contact: clinicaltrials@cunet.carleton.ca

Pathway Options: Coursework, Practicum

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