In this role, you will manage local Monitors, supervising clinical monitoring and site management activities to verify the protection of trial subjects’ rights, safety and well-being, data quality and study compliance on a country/regional level.Only CVs in English will be considered.You will:Facilitate regional projects as Lead Monitor and supervise study activities, timelines and schedulesTrain Monitors in annotated monitoring visit reportsReview monitoring reports and support monitors in their activitiesAct as the main communication line between Monitor and Regional LeadFacilitatesite budgets and contract negotiationsBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progress and lead project team calls on the country levelParticipate in quality control and compliance monitoringMay need to monitor and manage sites (if applicable)May need to supervise monitors on siteOversee and maintain study-specific and corporate tracking systems at site and country level