As clinical research coordinator, Laura must arrange the research study site, oversee recruitment and screening and enrollment of clinical study participants. She also schedules participant follow up visits. Laura is responsible for maintaining and dispensing the investigational product and other study supplies. She must complete and ensure the accuracy of case report forms. She further ensures site-wide adherence to Good Clinical Practice guidelines. Her role as Regulatory Coordinator also maintains the regulatory binder, completes and submits regulatory documents per sponsor requirements and updates IRB when needed. She also completes such tasks as updating IRB when needed, ordering study supplies, scheduling CRA monitoring visits, entering data into EDC, answering sponsors within 24 hours, among others. Laura also performs patient and family teaching to promote health and prevent complications.