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As a Medical Advisor at Novartis, you will play a strategic role in shaping the medical positioning of both marketed and pipeline compounds within your assigned therapeutic area. You will act as a key scientific expert, providing up-to-date medical insights and driving Novartis’ scientific messaging to both internal and external stakeholders. In close collaboration with Country, Regional, and Global teams, you will co-design the clinical development, launch strategy, and lifecycle management of assigned products. You will contribute to the implementation of local and global therapeutic area strategies through innovative and integrated evidence generation. Additionally, you will be responsible for the planning and execution of medical projects and events, ensuring alignment with medical strategic objectives and always placing the needs of patients and those who care for them at the center of your work.

Key responsibilities:

Your responsibilities include, but are not limited to:

• Strategic Support for Drug Development and Lifecycle Management: provide strategic medical input to the development, registration, launch, and lifecycle management of assigned pipeline and marketed compounds, ensuring alignment with both local and global therapeutic area strategies.
• Scientific Guidance Across Internal Functions: act as a medical and scientific expert by supporting various internal stakeholders—including regulatory, market access, marketing, and clinical teams—ensuring consistent and high-quality scientific communication.
• Cross-functional and Cross-regional Collaboration: collaborate effectively with local, regional, and global Medical Affairs, Global Drug Development (GDD), Patient Advocacy, and Public Affairs teams to drive aligned and impactful execution of medical plans and initiatives.
• Clinical Studies and Scientific Publications: contribute to the planning, execution, and oversight of global, regional, and local clinical studies. Support timely and compliant scientific dissemination through publications, adhering to GCP, ICH, and local regulations.
• Evidence Generation and Real World Data Initiatives: identify Real World Evidence (RWE) needs and lead the implementation of innovative evidence-generation approaches to bridge knowledge gaps, support patient access, and improve clinical outcomes.
• Scientific Training and Educational Leadership: develop and deliver tailored scientific training and disease/product education for internal teams (e.g., field force, MSLs) and external partners, ensuring accurate and up-to-date communication of clinical data.
• Medical Governance, Ethics, and Compliance: ensure that all medical activities comply with ethical standards, corporate policies, and local regulations—including oversight of safety reporting, GCP adherence, and review of promotional and non-promotional materials.
• Medical Projects and Budget Oversight: lead or contribute to the planning and execution of non-promotional medical initiatives and scientific events. Manage assigned Medical Affairs budgets efficiently, and when required, lead cross-functional medical project teams.

Essential Requirements

• MD Degree
• English and Italian: Proficient
• Good planning skills
• Good negotiation skills
• Medical and scientific writing skills
• Good communication skills
• Team player in a matrix organization.

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