Business Area: R&D;, Pharmacovigilance & Regulatory Affairs

Job Type: Direct Employee

Contract Type: Permanent

Location: Italy, IT

Responsibilities
- End to end execution of assigned innovation and initiatives, translating strategies and study designs on time, quality, and compliant delivery across programs, therapeutic areas and geographies
- Ad hoc member of Integrated Clinical Teams, supporting cross functional alignment among Clinical Development, Clinical Evidence & Epidemiology, Digital Health, Medical Affairs & Patient Engagement
- Operational planning, coordination and delivery of clinical innovation and real world evidence (RWE) projects on secondary data use, within the Global Clinical Development governance framework
- Execute assigned clinical innovation, RWE, epidemiology, and database driven evidence projects in line with approved evidence strategies and pipeline priorities
- Translate approved concepts, protocols, and innovation designs into operational project plans, ensuring feasibility, scalability, and compliance

- Support implementation of approved innovation initiatives within ongoing development programs
- Participate in Integrated Clinical Team (ICT) activities for assigned programs, providing operational input and execution updates
- Support evidence and innovation decision making by translating strategic requirements into practical timelines, resource plans, and deliverables
- Ensure coordination and information flow across involved functions and stakeholders
- Coordinate and manage RWE studies and secondary data collection initiatives (regulatory and non regulatory) across the product lifecycle and geographies, under appropriate scientific oversight
- Support protocol development, study design finalization, and implementation of RWE studies in collaboration with Clinical Evidence & Epidemiology and RWE leadership
- Ensure operational control of timelines, quality, and budget for assigned RWE projects
- Acts as connector and integration e

Clinical Innovation Project Manager

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