This course explores how molecular discoveries move from the biobank to the bedside, becoming validated tools doctors can actually trust. You'll see how researchers test whether a biological signal is more than a lab curiosity — proving it holds up statistically and clinically before it can guide real medical decisions. From there, you'll follow how vast biobanks of tissue and health records feed into the design of human clinical trials, where safety, ethics, and rigorous protocol shape every step from Phase 0 through Phase IV. Finally, you'll explore how researchers comb through the genome itself, sifting millions of genetic variants to find the small handful that actually cause disease and can be turned into new therapeutic targets. By the end of the course, you'll understand the full journey a discovery takes, from a raw genetic signal to a validated biomarker to an ethically sound clinical trial ready to reach patients. This course is especially useful for anyone curious about how modern medicine actually gets made, step by step, from the lab to the clinic.

Translational Medicine 3: Biobanking & Clinical Trials

Translational Medicine 3: Biobanking & Clinical Trials
This course is part of Translational Medicine Specialization

Instructor: Yi-Fan Chen
Access provided by CalArts
Recommended experience
What you'll learn
Explore how a promising biological signal is tested and validated before it can be trusted as a reliable clinical tool.
Analyze how large-scale biobanks and clinical trials work together to move research safely and ethically toward human treatment.
Evaluate how genetic data is traced back to its root causes, connecting a disease's origins to the tools used to detect and treat it.
Skills you'll gain
- Epidemiology
- Drug Development
- Informed Consent
- Biostatistics
- Health Informatics
- Healthcare Ethics
- Clinical Research Ethics
- Laboratory Testing
- Specimen Collection
- Specimen Preparation
- Statistical Methods
- Precision Medicine
- Clinical Research
- Medical Science and Research
- Research Design
- Specimen Processing
- Data Analysis
- Biotechnology
- Regulatory Compliance
- Clinical Trials
Details to know

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September 2026
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