• Support and lead the management of multi-center clinical research studies • Perform site monitoring visits for source document verification and assess site compliance • Coordinate and provide support for all aspects of study including protocol and site management • Develop and manage study metrics, providing training and mentorship to junior team members • Analyze trends in identified issues and author visit reports and letters • Oversee and manage operational aspects of clinical trial sites in conjunction with project teams • Collect and review essential documents for investigational sites • Serve as primary liaison for site management issues • Lead and train others in reviewing study site data and data reports • Perform all duties in compliance with standard operating procedures, federal guidelines, and other applicable laws • Develop, maintain, and present clinical trial and project specific training materials • Participate in training junior CRAs on moderately complex concepts, processes, and tasks