Allison Camp, PhD, is a Clinical Development Associate for UNC Lineberger Comprehensive Cancer Center at the University of North Carolina Chapel Hill. She assists investigators in developing documents associated with clinical trial development and maintenance including letters of intent, initial clinical trial protocols, and protocol amendments. Allison also acts as a liaison between pharmaceutical companies and the principal investigators, as needed, during trial development and during the life of the study. Allison drafts patient-facing materials including informed consent forms and performs quality assurance activities for both consent documents and clinical protocols within the team. In addition, Allison assists in the initiation and maintenance of Lineberger-sponsored INDs and IDEs, including providing regulatory strategy to investigators, drafting and submitting initial applications to the FDA, managing FDA communications, and drafting and submitting subsequent submissions to the agency through the lifespan of the related clinical studies. She also assists with single subject INDs within Lineberger.
Previously, Allison served as a Grant Writing Specialist/Scientific Consultant for Eva Garland Consulting. Allison completed her postdoctoral research at the Environmental Protection Agency within the Center for Public Health and Environmental Assessment with a focus on pollinator toxicology. Prior to her graduate studies she worked as a Fisheries Biologist contractor at the National Oceanic and Atmospheric Administration within the Ecotoxicology Program.
Allison received her PhD in Toxicology from North Carolina State University and a BS in Neurobiology and BA in Psychology from the University of Washington.
