Clinical Research Coordinator III

Required - CRNP or PA-C

Full time Clinical Research Coordinator for a large randomized controlled trial of treatment after resuscitation from cardiac arrest. Independently implements most research interventions required for the trial including screening and enrollment, obtains consent for participation or continued participation after enrollment with exception from informed consent, and reliably ascertains primary study outcomes. Completes accurate data collection, audits research studies, monitors study budgets, orders supplies, and resolves complex data collection issues. Prepares grant applications, manuscripts, Institutional Review Board (IRB) applications and adverse event reports and research manuscripts. Completes basic analyses (e.g., summary data reports) independently. Trains research staff, oversees student workers, leads project team meetings and working groups.