Kiley brings 14 years of regulatory medical writing experience and has supported clinical research studies and submissions across all phases of drug development (pre-IND, IND, NDA/BLA, and post-marketing). Kiley has supported investigational drug product classes including small molecules, cytokines, MAbs, peptibodies, and siRNA. Therapeutics areas supported have included oncology, hematology, immunology, endocrinology, infectious diseases, neuroscience, rare diseases, and vaccine development. Kiley enjoys close communication and seamless integration with client teams of all sizes to guide and train them in moving forward as a cohesive unit to effectively bring challenging projects to successful completion. Kiley earned a PhD in Microbiology and Immunology at the University of Oklahoma Health Sciences Center and worked as a biomedical researcher with a focus in histocompatibility and MAb development prior to entering the clinical research industry as a regulatory medical writer. Kiley currently lives with her husband and cat in Charlotte, North Carolina.