Clinical Research Coordinator
Current➢Perform assigned protocol tests and procedures with patients/study participants including T25FW, 9HPT, SDMT, LCVA, PASAT, MSFC, BICAMS, TUG, 2MWT, COWAT, ANAM, & Visual Acuity➢Collect, record, report and file patient study data and paperwork including adverse events, serious adverse events, and changes to concomitant medications➢Perform basic lab prep work such as labeling, processing, and shipping of research samples➢ Assist and perform study enrollment visits including the informed consent process based on FDA regulations and standards➢Manage clinical studies while training and delegating other research team members regulatory tasks➢Screen and conduct enrollment and follow-up visits for a Multiple Sclerosis registry➢Complete data entry for study visits that occurred utilizing Electronic Data Capture systems➢Assist and collaborate with on-site and remote monitoring visits➢Track patients’ clinical MRI, OCT & neurological examination appointments to warrant that patients are receiving necessary clinical care➢Update regulatory binders that helps organize studies to be in compliance with protocols➢Pre-screen patient charts for numerous enrolling research studies