Experienced in Immunology & Oncology with an established track record in developing therapeutic products from the pre-clinical stage through registrational. My experience includes 5+ years of combined Clinical Operations, Logistics, and Regulatory Affairs. In 2017, I began my career in the clinical field enrolling patients into gene therapy trials. I later pursued the biopharma industry where I have successfully managed the logistics of patient enrollment into multiple trials, supported high-quality regulatory submissions for INDs, BLAs, and supplemental BLAs, and have assisted with GCP inspections following marketing authorization applications.