Gain specialized knowledge in trial design, regulatory compliance and ethical standards to support safe, evidence-based medical research.
The part-time, 6-course Certificate in Clinical Research equips you with the foundational skills and regulatory knowledge essential for contributing to the success of clinical research. Delivered online in a flexible, blended format over 11 months, this program—developed in collaboration with experts from the pharmaceutical and healthcare sectors—prepares you to work across key phases of clinical research. In addition, it fulfills the educational requirements for obtaining the Certified Clinical Research Professional (CCRP) credential, as recognized by the Society of Clinical Research Associates (SOCRA).
Through applied learning, you’ll build practical competencies in:
- Clinical trial phases, protocols and operational processes
- Health Canada and global regulatory frameworks (e.g., GCP, ICH)
- Ethical considerations in research involving human subjects
- Data collection, analysis and reporting in clinical studies
- Roles and responsibilities across sponsor, site and CRO environments
Learn from Experts. Collaborate with Peers. Drive Medical Innovation.
This certificate is designed for professionals entering or transitioning into the clinical research field. You will:
- Learn from experienced clinical researchers and regulatory specialists
- Apply concepts in real-world case studies and team-based simulations
- Complete a capstone focused on clinical trial planning and oversight
- Earn a recognized credential that supports career mobility in health research