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Summary:
Contribuye, con una supervisión adecuada, a todos los aspectos de los ensayos clínicos globales para ofrecer resultados de estudio dentro de los estándares de programación, presupuesto, calidad/cumplimiento y rendimiento. Puede liderar aspectos específicos del proceso de ensayo clínico general. Contribuye a la excelencia operativa a través de la mejora de procesos y el intercambio de conocimientos.
About the Role:
Major accountabilities
Data Generation, Governance & Excellence
Ensures that all processes, systems and operational elements comply with internal policy, industry standards, country regulations and compliance metrics for the conduction of projects in MA (GxP activities such as Interventional and NIS/RWE, IIT, MAP, RC and other relevant activities in MA).
Provides oversight of vendors/third parties involved in the planning and execution of MA projects and programs.
Act as a Subject Matter Expert in regulatory and clinical supply processes.
Contributes, with appropriate oversight, to all aspects RWE Projects to deliver study outcomes within schedule,
budget, quality/compliance and performance standards.
Provides oversight of budgets across Evidence Generation and other MA projects, aligning business and scientific objectives with the company priorities.
Proactively identify root cause and implement action to improve future audit/inspection
Support to the Data Generation & Governance team in local audit & inspection readiness and execution.
performance and track deviation and support implementation/resolution of local CAPA.
Track deviation and support implementation/resolution of local CAPA.
Monitor and report KPI/KQI using existing General systems & tools.
Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt.
Ensure proper classification of medical activities, in collaboration with local ERC department, if needed.
Leadership & Culture:
Ensure an
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