**Job Overview**
Lead Clinical Research Associates are assigned to oversee multiple studies across various countries, ensuring timely delivery and progress. They will also be responsible for verifying sponsor requirements and procedures at a minimum of one study site.
**Key Responsibilities:**
* Oversee overall study monitoring plan compliance;
* Serve as primary point of contact for IQVIA CRAs and sponsor Project managers;
* Provide oversight of site monitoring data management activities;
* Review Monitoring Visit Reports;
* Pull data management reports; (initially 100% MVR review); lead follow-up on missing pages, outstanding queries;