Dr. Spence has been with Nuventra since the Spring of 2018. As a project manager and clinical pharmacology consultant, she has diverse cross functional experience from work in large pharma, biotechnology, and specialty pharma and an established track record of clinical and regulatory success within the pharmaceutical industry. Her experiences include planning, executing, and supporting nonclinical and clinical pharmacology studies. Dr. Spence also has experience with strategic planning and support of drug development programs (from nonclinical IND enabling studies through Phase 1 to late stage studies leading to marketing registration). During her time at Nuventra, Dr. Spence has helped support dozens of international and domestic clinical trials across numerous therapeutic areas (small molecule compounds and biologics).