KPS is looking for Oversight Monitor to join sponsor team. Small FTE approx 0.2 for this year.The primary responsibility of the (Clinical) Oversight Monitor (C)OM) is to ensure adequate Sponsor oversight of the conduct, monitoring and management of one or more clinical studies and assigned monitors at clinical study sites, within the assigned country or region.The (C)OM):contributes to development of the Overall Study Management Plan, the study level Site and Monitoring Plan and the Oversight Monitoring Plan.contributes to the definition of appropriate standards and quality indicators for site management and monitoring.ensures high quality conduct and execution of clinical studies at sites according to the protocol and study team and governance requirements in compliance with quality, regional and regulatory (GCP) standards.addresses issues identified with study conduct, monitoring and site management with Sponsor’s management, are appropriately communicated/escalated and follows up through resolution.May conduct oversight monitoring visits, co-monitoring visits, monitoring visit report reviews and other Sponsor oversight activities per applicable study plans, as needed.reviews the submission documents for IRBs/IECs and Health Authorities as appropriate for assigned sites/countries/region.may assist with translations or verification of translations.implements approved communication plans with external strategic partners or CROs.supports the collection of key study performance information, including study start-up metrics, enrollment, data collection timeliness/quality.reviews monitoring visit reports for finalization/consistency/issues according to study monitoring plan.utilizes available tools/systems to assess vendor and site performance.ensures inspection readiness at the study sites and follow up corrective/preventive actions.maintains good communication and working relationships with investigators, internal stake-holders and external services providers (CROs)