Central Monitor in LATAM

Perform centralized monitoring activities on assigned projects, evaluating study quality and integrity against protocols, SOPs, and regulations. Maintain internal systems, databases, and tracking tools while managing triggers and preparing i-site packs for sites and countries. Participate in study team meetings to verify information, triage data issues, and escalate quality concerns to the Centralized Monitoring Lead. Review subject-level data for accuracy regarding inclusion/exclusion criteria, adverse events, and endpoints, interacting with sites and CRAs to follow up on study milestones from start to close out. This home-based role supports IQVIA's global clinical research services by ensuring data readiness for next-level review across LATAM and North America projects.