At a Glance
- Tasks: Lead global labelling strategies and collaborate with cross-functional teams in oncology.
- Company: Join Novartis, a diverse and inclusive employer committed to innovation.
- Benefits: Flexible working options, competitive salary, and opportunities for personal growth.
- Other info: Be part of a supportive community dedicated to breakthroughs in healthcare.
- Why this job: Make a real impact on patient lives through clear and compliant labelling content.
- Qualifications: Experience in Global Labelling or Regulatory Affairs with strong communication skills.
The predicted salary is between 80000 - 100000 £ per year.
This job is with Novartis, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.
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.
About the Role
- 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.
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.
Global Labelling Associate Director, Content (Oncology) employer: Novartis
Novartis is an exceptional employer that fosters an inclusive and collaborative work culture, particularly in the vibrant setting of London. With a strong commitment to employee growth, Novartis offers numerous opportunities for professional development and mentorship, ensuring that every team member can thrive while contributing to meaningful advancements in oncology. The hybrid working model allows for flexibility, making it easier for employees to balance their personal and professional lives while being part of a community dedicated to improving patient outcomes.
StudySmarter Expert Advice🤫
We think this is how you could land Global Labelling Associate Director, Content (Oncology)
✨Network Like a Pro
Get out there and connect with people in the industry! Attend events, webinars, or even local meet-ups. The more you engage with others, the better your chances of hearing about opportunities that might not be advertised.
✨Show Off Your Skills
When you get the chance to chat with potential employers, don’t hold back! Share specific examples of your past work, especially those that relate to global labelling and regulatory affairs. This is your time to shine and show them what you can bring to the table.
✨Follow Up
After any interview or networking event, make sure to follow up with a thank-you email. It’s a simple gesture that shows your appreciation and keeps you on their radar. Plus, it’s a great opportunity to reiterate your interest in the role!
✨Apply Through Our Website
Don’t forget to apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at Novartis.
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 for the Global Labelling Associate Director role. Highlight your experience in global labelling and regulatory affairs, and show how your skills align with the job description. We want to see how you can contribute to our team!
Showcase Your Collaboration Skills:Since this role involves working closely with cross-functional partners, emphasise your teamwork and communication abilities. Share examples of how you've successfully facilitated discussions or aligned strategies in previous roles. We love a good team player!
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 labelling strategies.
Apply Through Our Website:Don’t forget to submit your application through our official website! It’s the best way for us to receive your details and ensure you’re considered for the role. Plus, it shows you’re serious about joining our team at Novartis!
How to prepare for a job interview at Novartis
✨Know Your Labelling Stuff
Make sure you brush up on global labelling strategies and core documents like CDS and USPI. Being able to discuss these confidently will show that you understand the role and can contribute from day one.
✨Show Off 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 resonate well with the interviewers.
✨Prepare for Health Authority Queries
Familiarise yourself with common Health Authority queries and think about how you would respond. This shows that you're proactive and understand the regulatory landscape, which is crucial for the position.
✨Emphasise Your Attention to Detail
In a role where accuracy is key, be prepared to discuss how you ensure high-quality work within tight timelines. Share specific examples of how your planning and prioritisation skills have led to successful outcomes in previous roles.
