Overview Works under the supervision of the Research Manager. Responsible for all aspects of research coordination for research studies; Responsible for research specific quality nursing care for patients participating in clinical trials. Responsibilities - Plan, implement and monitor participant recruitment and retention procedures. - Screen and interview study participants. - Interpret and implement protocol procedures and policy. - Maintain case report forms, charts and documentation. - Collect and enter research data in electronic data capture, review lab and procedure results. - Dispense study medication and maintain records. - Maintain regulatory compliance and documents as mandated by FDA regulations. - Open communication with study sponsors, Institutional Review Boards, and Research Office. - Assist study monitors and sponsors with site visits. - Assist audit services with internal study audits and reports. - Completes quality assurance assignments. - Arranges for study-related inpatient hospital services and assures that study related laboratory tests and diagnostic procedures are completed. Qualifications - 2 years Nursing Required - LPN license required - Bachelors Preferred