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

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

London Full-Time 67900 - 126100 £ / year (est.) Home office (partial)
Meeveem Limited

At a Glance

  • Tasks: Lead the development of global labelling content for established medicines.
  • Company: Join Novartis, a leader in innovative healthcare solutions.
  • Benefits: Competitive salary, performance bonuses, flexible working, and generous parental leave.
  • Other info: Collaborate with diverse teams and enjoy excellent career growth opportunities.
  • Why this job: Make a real impact on patient safety and healthcare decisions globally.
  • Qualifications: Degree in a scientific discipline and experience in global labelling content.

The predicted salary is between 67900 - 126100 £ per year.

Location: London, United Kingdom (Remote for those residing in the UK, but more than 50 miles from the office). This role is based in London (The Westworks), United Kingdom or Remote. Novartis is unable to offer relocation support: please only apply if accessible.

Great medicines deserve clear, compelling storytelling. As a Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism), you will play a pivotal role in shaping how critical product information is communicated across global markets. Working at the intersection of science, strategy, and regulatory excellence, you will lead the development of high-quality global labelling content that supports patient safety, regulatory compliance, and commercial success. This is an opportunity to influence important healthcare decisions, collaborate with diverse international experts, and make a meaningful impact on established medicines that continue to improve patients' lives worldwide.

Key Responsibilities:

  • Develop and maintain global labelling strategies and content for established products across development and lifecycle activities.
  • Lead cross-functional discussions to achieve alignment on global labelling strategy, content, and key product claims.
  • Drive the creation and maintenance of core and major market labelling documents.
  • Present labelling recommendations, updates, and strategic proposals to governance bodies and project teams.
  • Anticipate emerging labelling risks and develop mitigation, escalation, and contingency plans.
  • Support health authority interactions by preparing evidence-based responses and negotiation strategies.
  • Mentor colleagues and contribute to continuous improvement, inspection readiness, and knowledge sharing initiatives.

Essential Requirements:

  • Degree in a scientific discipline with strong understanding of pharmaceutical development and regulatory requirements.
  • Experience developing and maintaining global labelling content for medicinal products across the product lifecycle.
  • Ability to interpret clinical efficacy and safety data and translate findings into clear labelling content.
  • Strong knowledge of global labelling regulations and requirements across major health authorities.
  • Proven ability to collaborate effectively across multidisciplinary teams and influence diverse stakeholders.
  • Excellent planning, prioritisation, communication, and attention to detail with a focus on quality.

Benefits & Rewards:

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. Expected Annual Base Salary Range for role: £67,900 to £126,100. The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. You may be eligible for a company vehicle or a car allowance in accordance with the applicable local Novartis policies and guidelines. Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

Commitment to Diversity and Inclusion: 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 (Cardiovascular, Renal & Metabolism) London employer: Meeveem Limited

Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.

Meeveem Limited

Contact Details:

Meeveem Limited Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism) London

Unlock Networking Opportunities

Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Meeveem Limited. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.

Join Relevant Professional Bodies

Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Meeveem Limited.

Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Meeveem Limited. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.

Tailor Your Approach

When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Meeveem Limited is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism) London

Global Labelling Strategy Development
Regulatory Compliance
Pharmaceutical Development Knowledge
Clinical Data Interpretation
Labelling Content Creation
Cross-Functional Collaboration
Stakeholder Influence

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Meeveem Limited!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Meeveem Limited that you're not just a fit for the job but also a safety-conscious candidate!

Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Meeveem Limited!

Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Meeveem Limited, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.

How to prepare for a job interview at Meeveem Limited

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Meeveem Limited that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

Know Their Products

Take some time to familiarise yourself with Meeveem Limited’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.

Be Ready for Regulatory Scenarios

In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.