Larry J. Davis, Pharm.D.

With 25+ years of experience in pharmaceutical and biotech leadership, I support life sciences teams in clinical, medical, and regulatory strategy with a strong focus on execution quality and compliance. My work centers on medical and clinical affairs, regulatory planning, drug safety/pharmacovigilance, and quality systems across development and commercialization contexts. He is publicly listed as Professor of Practice in Clinical and Regulatory Affairs at Keck Graduate Institute and has also held senior leadership roles in industry, including multiple VP positions (such as medical/clinical affairs and quality/compliance) and independent consulting work for pharma/biotech organizations. He also contributes thought leadership on FDA policy, pharmacovigilance, and regulatory topics through recent industry commentary and LinkedIn posts.