Kirsten has been with TOI since 2011, when ICRI was established. Prior to joining TOI, Kristen spent six years as a clinical research coordinator in dialysis, internal medicine, and oncology. Her whole 17-year career has been in clinical research. She is certified as a clinical research professional and has overseen more than 1,000 clinical trials. As a project manager, she has contributed to the growth of ICRI. She oversees all aspects of a clinical trial, from site selection to the close-out visit. She trains and supervises her staff to make sure they adhere to FDA regulations and GCP guidelines. Kirsten strives to provide excellence to both pharmaceutical companies and the patients that participate in the clinical trials.