Ms. Turner is a Clinical Research Coordinator who is knowledgeable in regulatory and human subject research issues. Her primary focus on participant protection encompassing diverse study requirements, such as grantsmanship, protocol approvals, advertising, recruitment, screening, consenting, data record management, and Data Safety Management Plans. Her previous experience includes Project Manager, reconciliation, auditing, and the day-to-day management staff members, as well as protocol compliance supervision of a large staff comprised of researchers, physicians, technicians, and nurses.