Clinical Research Nurse Coordinator

Description: Prepares materials for approval by ACRI and the applicable IRB.Conducts screening procedures for study enrollment. Recruits subject for participation and obtains consent/assent for research participation. Prepares flowcharts, study specific source documents and other study related materials. Assures clinical interventions are administered per protocol. Collects/records subject data on the case report forms using source documentation. Serve as a clinical/research resource to subjects, families, and other healthcare providers regarding the needs of the study and subject/family. Collaborates with other caregivers, research team members, and subject/family in planning, implementing, and evaluating research activities. Performs other duties as assigned.