Global Labelling Content Lead - Remote/Hybrid

Novartis AG; United States; Híbrido; USD 76 000 - 140 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Insurance plans

Retirement plans

Wellbeing resources

Global recognition programs

Hybrid working

Paid parental leave

Car allowance

Resumo da oferta

Novartis AG is seeking a Global Labelling Manager, Content, to develop clear, compliant product labelling for neuroscience medicines across global markets. You will translate complex clinical data into accessible labelling and work with regulatory, medical, and commercial teams to ensure alignment and audit-ready documentation.

The role combines science, regulation and strategy, with hybrid working options between London/UK offices and remote UK-based work.

Qualificações

• Degree in a scientific discipline or equivalent experience in pharma/labelling.
• Experience developing/regulatory labelling content for medicinal products.
• Strong understanding of global labelling principles and major market requirements.
• Ability to translate clinical/safety data into clear product information.
• Excellent collaboration and communication across cross-functional teams.

Responsabilidades

• Lead development and maintenance of global labelling documents.
• Prepare high-quality labelling content aligned with regulatory requirements.
• Facilitate cross-functional labelling discussions and drive alignment.
• Evaluate clinical and safety data to support labelling updates.
• Support responses to Health Authority enquiries with accurate information.
• Ensure timely implementation of labelling changes across markets.
• Maintain documentation, traceability and version control for audit readiness.

Conhecimentos

Regulatory labelling

Global labelling

Stakeholder management

Clinical data interpretation

Cross-functional collaboration

Formação académica

Degree in a scientific discipline

Descrição da oferta de emprego

Novartis AG is seeking a Global Labelling Manager, Content, to develop clear, compliant product labelling for neuroscience medicines across global markets. You will translate complex clinical data into accessible labelling and work with regulatory, medical, and commercial teams to ensure alignment and audit-ready documentation.

The role combines science, regulation and strategy, with hybrid working options between London/UK offices and remote UK-based work.