Clinical Trials York University

Program Description

The clinical research industry is rapidly evolving, and the demand for professionals with advanced data management and analysis skills in clinical trials has never been higher. The Post-Graduate Certificate in Clinical Trials is an in-person, four-day-a-week program designed to allow graduates to gain GCP (Good Clinical Practice) Certification in only eight months. This comprehensive program covers timely, relevant, and innovative topics, including clinical trial monitoring, research operations, design and planning and critical data analysis programming, ensuring graduates are well-equipped to hit the ground running and thrive in the growing and dynamic field of clinical trials. What You Will Learn Deepen Scientific & Analytical Expertise – Gain expertise in GCP-certified methodologies, clinical data management, immunology, microbiology and advanced data analysis techniques. Master Cutting Edge Data Systems – Gain hands-on experience with industry-standard EDC platforms, eCRF design and automated query resolution using risk-based approaches. Explore Immunology & Microbiology – Understand how these sciences impact clinical trials and drug development. Navigate Regulations & Ethics – Gain a deep understanding of industry standards, ethical considerations and compliance requirements. Leverage AI & Emerging Technologies – Explore how artificial intelligence, machine learning and digital health tools are transforming clinical data management. Master Cross-Functional Collaboration – Develop strategies for effective communication between data managers, medical monitors and data scientists to optimize trial efficiency and data quality.

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