Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

Summary

#LI-Hybrid (12 days per month on-site if living within 50 miles of our London office)
#LI-Remote (Homeworker if living further than 50 miles of our London office)
Office Location: London (The Westworks), United Kingdom

We are looking for a Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism) to contribute to the development and delivery of global labelling strategies across a portfolio of products.

In this role, you will support the creation of clear, consistent, and scientifically robust labelling content across development and lifecycle stages. You will work closely with cross-functional partners to ensure alignment on labelling strategy, enabling compliant and competitive product information for global markets.

About the Role

Major Accountabilities

• Develop and maintain global labelling strategies and core labelling documents for assigned products (e.g. CDS, USPI, EU SmPC/PIL).
• Lead and facilitate cross-functional discussions to support alignment on labelling content and strategy.
• Present labelling proposals and updates to governance bodies and project teams
• Identify emerging labelling considerations and contribute to planning, risk assessment, and mitigation strategies.
• Analyse competitor labelling, regulatory guidance, and scientific data to inform content development.
• Support and contribute to responses to Health Authority queries and interactions, including preparation of supporting documentation.
• Collaborate with global and regional partners to ensure consistency and alignment across markets.
• Mentor colleagues and contribute to audit readiness, inspections, and continuous improvement initiatives.

Essential Requirements

• Fluency in English (written and spoken).
• Demonstrated capability in Global Labelling and/or Global Regulatory Affairs, with a focus on labelling across development and lifecycle activities.
• Ability to develop and maintain core labelling documents (e.g. CDS) and support major market labelling (e.g. USPI, EU SmPC/PIL) with scientific accuracy and compliance.
• Ability to interpret clinical efficacy and safety data and translate it into clear, consistent labelling content and supporting documentation.
• Working knowledge of global labelling standards and expectations, including major Health Authority requirements.
• Strong collaboration and communication skills, with the ability to facilitate cross-functional discussions and support alignment.
• Strong planning, prioritisation, and attention to detail to deliver high-quality work within timelines.

Commitment to Diversity and Inclusion / EEO paragraph

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?

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