Lead Clinical Research Associate - (Raritan, NJ)

Lead Clinical Research Associate needs 5+ years of site managerial experience and a min of two years field monitoring background Lead Clinical Research Associate requires: BS/BA, MS is desirable Knowledge of applicable standards and regulations for clinical trials Proven planning skills; expertise to create and track detailed project plans Expertise to operate independently and within a cross-functional team environment to identify and escalate site/monitoring related activities issues to the management team in a timely fashion Cardiovascular Therapeutic area In Vitro Diagnostic Study Background Medidata RAVE system Lead Clinical Research Associate duties: Assisting with overall clinical site management for the lifecycle of the assigned trial Assisting with the maintenance of the Trial Master File to ensure completeness Serves as a resource to site coordinators, investigators, and other staff members regarding the execution of the trial