Tamia Dixon

Background

About Tamia Dixon

I am an Epidemiologist with over 6 years of experience in public health, regulatory compliance, and healthcare quality programs, now transitioning into the pharmaceutical industry. My background includes leading national surveillance initiatives with the CDC, managing regulatory submissions, and authoring peer-reviewed publications that inform evidence-based decision-making.Skilled in regulatory affairs, pharmacovigilance, clinical data management, and real-world evidence (RWE) generation, I bring a proven ability to analyze complex datasets, ensure data integrity, and translate scientific findings into actionable insights for diverse stakeholders. My expertise spans FDA/OMB compliance, adverse event monitoring, scientific communications, and cross-functional project leadership.I am particularly passionate about bridging epidemiology and clinical research to support drug development, safety monitoring, and medical affairs. With advanced technical skills in SAS, R, Tableau, and REDCap, I design data-driven solutions that improve processes and enhance compliance outcomes.I am excited to contribute my regulatory knowledge, medical writing experience, and public health expertise to advance innovative therapies and ensure patient safety in the biopharmaceutical space.