Clinical Research Coordinator
April 2012 — Present
Creates/transcribes correspondence, reports, manuscripts, and other documents and related materials to study.Point contact on all protocol guidance eligibility compliance, comprehension, and clinical translation. Provides planning and coordination of all protocol related meetings, including travel and lodging negotiations. Draft/edit all clinical documents, CRFs, manuals, presentations as needed.Contact person for protocol violations and serious adverse event reporting.Create, edit, and update Standard Operating Procedures (SOP).Assist in website development, including on-going updates.Explain study and obtain informed consent to enroll patients on research study, schedules patients for exams and tests in accordance with study protocol, monthly telephone follow-up with patients,performs electronic data entry of all required case report forms, prepare and ship biological specimens to repository site and/or laboratory, maintain supplies of forms, patient incentives and other supplies required by protocol.