Key ResponsibilitiesEnsure compliance of GLP, GCP, GVP and Regulatory Affairs systemsMaintain compliance frameworks, SOPs, policies and guidanceSupport system selection, onboarding, validation and oversightManage deviations, investigations, CAPAs and inspection-readiness activitiesProvide QA oversight for computerized systems lifecycle activitiesData Integrity GovernanceEnsure end-to-end Data Integrity across clinical and PV data flowsImplement ALCOA+ principles, audit trails and metadata controlsAssess DI risks across external vendors, integrations and interfacesSupport dataflow mapping and transfer controlsDrive continuous improvement aligned with ICH E6(R3) and EMA expectations