Summary:   The Clinical Research Associate (CRA) is responsible for clinical monitoring activities as part of a clinical trial team.  The CRA serves as liaison between the Project Manager (PM), Clinical Trial Assistants (CTAs), Clinical Trial Specialists (CTSs) and clinical trial sites.  They are integral in the documentation capture process ensuring all information is secured and accurate at both site and CRO levels.     Primary Responsibilities:  •    Travel to clinical trial sites to provide clinical monitoring throughout the lifecycle of a pharmaceutical or device study from feasibility determination to close-out•    Supervises on-site conduct of clinical studies acting as liaison between Project Manager and si