Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation of regulations, guidelines, policies, and procedures. Support management in promotion and assessment of compliance to regulations, guidelines and corporate policies. Essential Functions Plan, schedule, conduct, report and close audit activities in any of the countries involved with IQVIA contracts to assess compliance with applicable regulations/guidelines, customer requirements, IQVIA SOPs and project specific guidelines/instructions Evaluate audit findings and prepare and distribute reports to operations staff, management, and customers Provide interpretation and consultation to project teams on regulations, guidelines, compliance status, and policies and procedures Provide consultation to customers and monitors in interpretation of audit observations and formulation of corrective action plans Review,
approve investigations, Root Cause Analysis (RCA), Corrective Action Prevention (CAPA) and Effectiveness Check (EC) plans and track till closure for quality events arising from Audits; and from Quality Issues, Inspections or during similar QA activities as assigned. Evaluate policies and procedures for compliance with applicable regulations/guidelines and provide recommendations to management for continuous process improvements Maintains the electronic quality management system (e QMS) and provides support in relation to the audit lifecycle Lead/collaborate/support in QA initiatives/projects for quality, process improvements Assist in training of new Quality Assurance staff May be required to manage Quality Issues May present educational programs and provide guidance to operational staff on compliance procedures May perform pre-inspection visits at sites, host audits/inspections; ensure proper conduct
📌 Senior qa auditor (Italia)
🏢 Iqvia
📍 Italia