Over eighteen (18) years of experience in Clinical Research with experience in clinical study start-up, maintenance, and close-out for clinical research studies, including industry, federally sponsored, and locally (investigator) sponsored research. Experienced in Trial Master File management, maintenance, and reconciliation; regulatory submissions; data query resolution; creation and procurement of study-specific data and documents; Utilize CTMS to create study calendars and optimize patient treatment and tracking of study procedures for nationally recognized research institutions. Strengths include exceptional organizational skills and sharp attention to detail, ability to communicate and work efficiently within a team environment, problem-solving skills, and a demonstrated experience interacting with clients and providing timely status updates both from an internal and external standpoint. Therapeutic areas of experience include Pulmonary Disease, Lung Transplantation and Oncology.