Amy Robinson, PhD

Amy Robinson, PhD

Director, Regulatory Affairs

Dr. Robinson has 3+ years of experience in medical writing, specifically related to oncology and early phase clinical trial protocols.  Prior to joining Dunn Regulatory Associates, Dr. Robinson was a Medical Writer at Technical Resources International, Inc.  Before moving to Medica Writing, she was involved in non-clinical academic research in neuroscience.  She holds a Ph.D. in Pharmacology and Biomedical Neuroscience with a concentration in neuroanatomy from Boston University and a BS in Chemistry from University of Florida.