Clinical Research Coordinator, RN

Monitor the overall day-to-day conduct of assigned early phase oncology studies in accordance with protocols, Standard Operating Procedures, and Good Clinical Practice. Create or review forms for assigned trials to ensure compliance, maintain standardized study files, and implement initial protocol amendments while training relevant staff. Facilitate informed consent processes, assist with patient screening and eligibility determination, and perform telephone triage assessments when necessary. Prepare and manage source documents, assist the data coordinator with case report form completion and query resolution, and work with the Principal Investigator to submit Serious Adverse Event reports. Recognize protocol deviations and address corrective actions to prevent future issues, ensuring all team members adhere to assigned protocols. Provide patient education regarding trial participation, chemotherapy administration, and potential side effects.