At a Glance
- Tasks: Lead global labelling strategies for oncology products and collaborate with cross-functional teams.
- Company: Join Novartis, a leader in healthcare committed to diversity and inclusion.
- Benefits: Flexible working options, competitive salary, and opportunities for professional growth.
- Other info: Work in a dynamic environment with excellent career advancement opportunities.
- Why this job: Make a real impact in oncology by ensuring clear and compliant product information.
- Qualifications: Experience in global labelling or regulatory affairs with strong communication skills.
The predicted salary is between 80000 - 100000 £ per year.
We are looking for a Global Labelling Associate Director, Content (Oncology) 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.
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.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Global Labelling Associate Director, Content (Oncology) in London employer: Novartis UK
At Novartis, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of oncology labelling. With flexible working arrangements, including the option to work from home for those living further than 50 miles from our London office, we prioritise employee well-being and work-life balance. Our commitment to professional growth is evident through mentorship opportunities and a focus on continuous improvement, making Novartis a rewarding place to advance your career while contributing to meaningful healthcare solutions.
StudySmarter Expert Advice🤫
We think this is how you could land Global Labelling Associate Director, Content (Oncology) in London
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those who work at Novartis or similar companies. A friendly chat can open doors and give you insights that might just help you land that Global Labelling Associate Director role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of global labelling strategies and regulations. We recommend practising common interview questions and having examples ready that showcase your experience in developing core labelling documents.
✨Tip Number 3
Showcase your collaboration skills! In your discussions, highlight how you've successfully worked with cross-functional teams in the past. This is key for the role, so make sure to emphasise your ability to align on labelling content and strategy.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in joining our team and contributing to the exciting work we do in oncology.
We think you need these skills to ace Global Labelling Associate Director, Content (Oncology) in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Global Labelling Associate Director role. Highlight your experience in global labelling and regulatory affairs, especially in oncology. We want to see how your skills align with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about labelling strategies and how you can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Collaboration Skills:Since this role involves working closely with cross-functional partners, make sure to highlight your collaboration and communication skills. Share examples of how you've successfully facilitated discussions or aligned teams in the past.
Apply Through Our Website:Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts!
How to prepare for a job interview at Novartis UK
✨Know Your Labelling Strategies
Make sure you brush up on global labelling strategies and core labelling documents relevant to oncology. Be prepared to discuss how you would develop and maintain these documents, as well as your experience with CDS, USPI, and EU SmPC/PIL.
✨Showcase Your Collaboration Skills
This role requires strong collaboration with cross-functional teams. Think of examples where you've successfully facilitated discussions or aligned strategies with different departments. Highlight your communication skills and how they helped achieve project goals.
✨Prepare for Regulatory Questions
Since you'll be dealing with Health Authority queries, it’s crucial to understand the regulatory landscape. Familiarise yourself with major Health Authority requirements and be ready to discuss how you've navigated these in past roles.
✨Demonstrate Attention to Detail
Attention to detail is key in this position. Prepare to give examples of how you've ensured accuracy in labelling content and documentation. Discuss any processes you’ve implemented to maintain high-quality work within tight timelines.
