Clinical Research
| Study location | Canada, Ontario, Toronto |
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| Type | Graduate Certificate, College |
| Nominal duration | 1 year/ 3 semesters |
| Study language | English |
| Course code | 07681 |
| Tuition fee | CA$28,603 per year The fees are for the 2024–2025 academic year and include tuition (CA$26,260), health insurance and ancillary charges. The fees displayed are estimates for three semesters and are subject to change. |
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| Registration fee | CA$375 one-time The registration fee includes the non-refundable application fee (CA$75) and the refundable deposit fee (CA$300). Please REVIEW the EdviseCanada`s fee policy. |
| Entry qualification | Undergraduate Diploma (or higher) To be eligible for admission, you must possess:
Note: This program does not offer a conditional admission for applicants who do not meet the English language requirements. The entry qualification documents are accepted in the following languages: English. |
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| Language requirements | English For direct admission, if English is not your first language, OR you did not complete a minimum of two full years of successful study in an accredited university degree program/college diploma program in a country OR in a postsecondary institution where English is the primary language of instruction, you must provide one of the English language proficiency tests below:
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Overview
Embark on an engaging educational journey in clinical research with our comprehensive online program, structured over three semesters. Immerse yourself in curriculum meticulously designed to cultivate the vital skills required to flourish in the dynamic realm of clinical research.
Humber’s Clinical Research graduate certificate program prepares graduates with the transferable skills needed to build successful careers in a variety of clinical trial management and research sectors. This program focuses on developing the concepts, skills and techniques required to work in the clinical research field. You will gain knowledge and skills in the planning and management of clinical research including practices related to the organization, execution and monitoring of clinical trials. You will learn clinical trial protocol development as part of the principles and processes of clinical trial design.
There is an emphasis on maintaining good clinical practice (GCP) as presented by the International Conference on Harmonization (ICH), along with the importance of data collection, analysis, recording and auditing – all to ensure that clinical trial data are credible and accurate. You will become familiar with the many regulations and guidelines established to ensure trials are conducted ethically and in ways that respect the rights of clinical trial participants, while ensuring the execution of robust scientific research.
Teamwork and communication skills are reinforced throughout the program, and you will acquire the necessary technological skills to assist with data management specific to the field.
You will also benefit from:
- a unique integrated approach
- acquiring a recognized skillset applicable to a wide variety of employment opportunities
- integrative project work that links applied and academic fields
- learning to adapt to the changing field and staying current
- simulation trials mimicking real work experiences
Career opportunities
Graduates typically pursue careers in research settings such as:
- pharmaceutical,
- medical device and biotechnology industries,
- hospitals, and
- research institutes.
Their work may help lead to the development of new treatments and therapeutic approaches to enhance quality of life.
Join on this enriching journey where this program not only accommodates the demands of a full-time schedule but also emphasizes the critical hands-on experience gained during the field experience. Elevate your career prospects, contribute significantly to medical science and navigate this intensive and rewarding educational pathway.