**Job Overview**

Lead the execution of Centralized monitoring activities at multiple sites and studies from initiation through to closeout. Ensure that completion of work, clinical study management and project deliverables are on time and is in accordance with SOPs, policies and Good Clinical practices and applicable regulatory requirements. To provide CMS related support and assistance across multiple projects, sites and teams and review the structured clinical data output with access to medical charts. Adherence to protocol, overall completeness, and readiness of the supplied patient information to the next level of patient review and support the CMS leads in defining the metrics and timelines. Facilitate efficient and effective review of Site Visit Reports and assure consistent standards of implementation for quality to meet or exceed quality standards. Ensure subject safety, data integrity, escalation of issues and timely and responsive feedback in compliance with IQVIA SO...