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Become a clinical trial specialist
Clinical Research
Learn ICH-GCP, study design, monitoring, and the trial lifecycle from protocol to closeout — guided by a Canada-based clinical lead.
Duration
4 weeks
Schedule
EST
Certificate
Not included
Apply by
June 1, 2026
What you'll learn
- ICH-GCP and Health Canada regulatory framework
- Protocol design, CRF design, and study feasibility
- Site monitoring and source data verification
- Adverse event reporting and safety oversight
- Sponsor / CRO collaboration in real workflows
Curriculum
Weekly modules with live sessions, recordings, hands-on labs, and 1:1 reviews.
Who this is for
Best for
Pharmacy graduates, life-sciences postgrads, healthcare professionals pivoting into research.
You'll be ready to be
Career changers entering CRA / CRC roles in Canada.
Frequently asked
Yes — every live class is recorded and added to your dashboard within 24 hours so you can revisit any topic at your own pace.