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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.
Programme overview
Main Subject
Health/Healthcare
Degree
MSc
Study Level
Masters
Study Mode
On Campus
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.
Scholarships
Selecting the right scholarship can be a daunting process. With countless options available, students often find themselves overwhelmed and confused. The decision can be especially stressful for those facing financial constraints or pursuing specific academic or career goals.
To help students navigate this challenging process, we recommend the following articles:
Master of Science in Clinical Trials and Regulatory Affairs
Main Campus, Ottawa, Canada
Health/HealthcareMain Subject Area
Programme overview
Main Subject
Health/Healthcare
Degree
MSc
Study Level
Masters
Study Mode
On Campus
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.
Programme overview
Main Subject
Health/Healthcare
Degree
MSc
Study Level
Masters
Study Mode
On Campus
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.
Scholarships
Selecting the right scholarship can be a daunting process. With countless options available, students often find themselves overwhelmed and confused. The decision can be especially stressful for those facing financial constraints or pursuing specific academic or career goals.
To help students navigate this challenging process, we recommend the following articles:
How to get a full scholarship
Looking for a fully-funded scholarship to see you into university? Find out how to boost your chances of getting one.
Scholarships to study abroad
Find scholarships to study abroad with our lists of international scholarships – categorized by country, by subject, and by type of student.
Scholarship Applications: Frequently Asked Questions
Get answers to all your questions about scholarship applications, including tips on how to find scholarships and chances of success.
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