Medical Devices and Diagnostics Research

Oncology clinical trials

The Clinical Research Coordinator is responsible for the identification, consent process and randomization, administration of study drugs. I monitors eligible patients enrolled in research protocols in accordance with FDA required Good Clinical Practice. I adhere to National Patient Safety Goals as appropriate based on the level of patient contact this position requires. I identify patients for clinical studies; oversee protocol required assessments of labs, vital signs, test results and any adverse events for research patients during study participation; provides education for the staff, patients and their families regarding research protocols, study medications and clinical procedures;