Madeline Naylor Email and Phone Number

Served as the lead clinical research coordinator for the Longitudinal Early-Onset Alzheimer’s Disease (LEADS) study. LEADS is a multi-center research study. Managed the day-to-day operations at the Indiana University site. Lead coordinator conducts study visits, serves as a liaison for the site and the site monitors, and oversees all clinical study activities such as data entry, protocol compliance, recruitment, and maintaining patient data.

Facilitate, coordinate, and conduct phase I, II, III clinical trials in accordance with ICH/GCP and CRF guidelines under the direction of a principle investigator. Coordinate neurology research studies, including subject recruitment and identification, protocol adherence, regulatory authority communication, adverse event reporting, and data collection and management.

Worked among a team of dedicated research professionals to facilitate, coordinate, and conduct phase II and III clinical trials in accordance with ICH/GCP and CRF guidelines. Served as the primary coordinator for nine cardiovascular clinical trials and six oncology clinical trials, including subject recruitment and identification, protocol adherence, and data collection and management. Among the nine cardiovascular trials, served as the lead coordinator for a surgical Transcatheter Aortic… Show more Worked among a team of dedicated research professionals to facilitate, coordinate, and conduct phase II and III clinical trials in accordance with ICH/GCP and CRF guidelines. Served as the primary coordinator for nine cardiovascular clinical trials and six oncology clinical trials, including subject recruitment and identification, protocol adherence, and data collection and management. Among the nine cardiovascular trials, served as the lead coordinator for a surgical Transcatheter Aortic Valve Replacement clinical trial, assisting in both the less invasive TAVR procedures and the open-heart SAVR procedures. Acquired skills in data collection, surgical techniques, and patient care. Show less

Served as a liaison among patients, families, and a team of multidisciplinary physician specialists to coordinate research studies involving hereditary dementia illnesses in accordance with standard operating procedures and GCP guidelines. Coordinated hereditary dementia research studies, including identification and recruitment of subjects, conducted subject visits with protocol-designated procedures, arranged genetic counseling sessions, and developed genetic pedigrees for study participants.

Assisted providers with surgical procedures, suture removals, preparing prescriptions, anesthetizing, bandaging, bacterial cultures, and biopsies. Provided instructions to patients regarding medical care as ordered by the provider