Dr. Evelyn Vance is a Biomedical Researcher and Clinical Data Scientist with a PhD in Epidemiology and 14 years of experience in pharmaceutical ethics and trial design. She specializes in demystifying complex health data, genetic privacy, and the regulatory frameworks of clinical research.
With a background spanning over a decade in both academic labs and private contract research organizations (CROs), Evelyn bridges the gap between dense scientific literature and public understanding. Her expertise covers the rigorous analysis of clinical trial phases, the statistical validation of health claims, and the ethical implications of genetic testing. She actively advocates for open science and teaches patients how to distinguish between peer-reviewed evidence and pseudo-scientific noise. Currently, she consults on patient consent protocols and data transparency for global health initiatives. Evelyn writes to empower readers with the tools to navigate medical decisions, understand risk correlations, and protect their biological data.