At a Glance
- Tasks: Lead global labelling strategies and create clear, compliant content for oncology products.
- 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 a focus on continuous improvement.
- Why this job: Make a real impact in oncology while collaborating with cross-functional teams.
- 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) 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 heart of London. Our commitment to employee growth is evident through mentorship opportunities and continuous improvement initiatives, ensuring that our team members thrive in their careers while contributing to meaningful advancements in oncology labelling strategies. With flexible working arrangements and a focus on diversity and inclusion, we create an environment where every voice is valued and every contribution makes a difference.
StudySmarter Expert Advice🤫
We think this is how you could land Global Labelling Associate Director, Content (Oncology)
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those who work in global labelling or regulatory affairs. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of global labelling strategies and regulations. Be ready to discuss how you can contribute to creating clear and compliant labelling content, as this will show you're the right fit for the role.
✨Tip Number 3
Don’t forget to showcase your collaboration skills! In your conversations, highlight examples of how you've successfully worked with cross-functional teams to align on labelling strategies. This is key for the role!
✨Tip Number 4
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 our mission in oncology labelling.
We think you need these skills to ace Global Labelling Associate Director, Content (Oncology)
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter to highlight your experience in global labelling and regulatory affairs. We want to see how your skills align with the role, so don’t hold back on showcasing your relevant achievements!
Showcase Your Collaboration Skills:Since this role involves working closely with cross-functional teams, it’s important to demonstrate your ability to collaborate effectively. Share examples of past experiences where you’ve successfully facilitated discussions or aligned strategies with others.
Be Clear and Concise:When writing your application, clarity is key! Use straightforward language and avoid jargon where possible. We appreciate well-structured content that gets straight to the point, especially when it comes to your understanding of labelling standards.
Apply Through Our Website:We encourage you to submit your application through our website for the best chance of being noticed. It’s the easiest way for us to keep track of your application and ensure it reaches the right people!
How to prepare for a job interview at Novartis UK
✨Know Your Labelling Stuff
Make sure you brush up on global labelling strategies and core documents like CDS, USPI, and EU SmPC/PIL. Being able to discuss these confidently will show that you’re not just familiar with the terms but can also apply them in real-world scenarios.
✨Showcase Your Collaboration Skills
Since this role involves working closely with cross-functional teams, be ready to share examples of how you've successfully facilitated discussions and aligned strategies in the past. Highlighting your teamwork will demonstrate that you can thrive in a collaborative environment.
✨Prepare for Health Authority Queries
Familiarise yourself with common Health Authority queries and think about how you would respond. Being prepared to discuss your approach to preparing supporting documentation will show that you understand the regulatory landscape and can handle challenges effectively.
✨Stay Updated on Competitor Labelling
Research competitor labelling and current regulatory guidance in oncology. Bring insights to the interview about how these factors influence labelling strategies. This will not only impress your interviewers but also show that you’re proactive and informed about the industry.
