Global Program Regulatory Director

Global Program Regulatory Director

Full-Time 51000 - 155090 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead global regulatory strategies and influence critical development decisions for innovative medicines.
  • Company: Join Novartis, a leader in transforming patients' lives through science and innovation.
  • Benefits: Competitive salary, performance bonuses, flexible working, and extensive wellbeing resources.
  • Other info: Diverse and inclusive work environment with excellent career growth opportunities.
  • Why this job: Make a real impact on global health by shaping regulatory strategies for life-changing medicines.
  • Qualifications: Bachelor’s or Master’s in a scientific field with significant regulatory affairs experience.

The predicted salary is between 51000 - 155090 £ per year.

Join Novartis as a Global Program Regulatory Director (GPRD) and play a pivotal role in shaping the global regulatory strategy for innovative medicines that have the potential to transform patients' lives. In this highly visible leadership role, you will influence critical development and commercialization decisions, guide complex Health Authority interactions, and bring together global stakeholders to navigate regulatory challenges and unlock opportunities.

Working at the intersection of science, strategy, and innovation, you will help drive successful product development across the lifecycle while contributing to Novartis' mission of reimagining medicine for patients worldwide.

Key Responsibilities

  • Develop and lead global regulatory strategies aligned to development, commercial, and portfolio objectives.
  • Lead Health Authority interactions to advance programs and achieve successful regulatory outcomes.
  • Evaluate regulatory opportunities and risks, implementing mitigation plans across global markets.
  • Provide strategic guidance on development plans, labeling, and key regulatory documentation.
  • Oversee regulatory submissions, ensuring high-quality dossiers and timely execution of deliverables.
  • Lead and influence cross-functional teams to drive aligned decision-making and program success.
  • Coach and develop regulatory team members while fostering collaboration, learning, and performance excellence.

Essential Requirements

  • Bachelor’s or Master’s degree in a scientific discipline; advanced degree preferred.
  • Significant regulatory affairs and pharmaceutical development experience across multiple stages of product development.
  • Proven expertise in developing and executing global regulatory strategies for complex programmes.
  • Strong experience leading Health Authority interactions, negotiations, and major regulatory submissions.
  • Demonstrated matrix leadership skills with the ability to influence cross-functional stakeholders globally.
  • Excellent communication, strategic thinking, problem-solving, and stakeholder management capabilities.

Benefits & Rewards

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. Long-term equity awards granted at group level may also be part of your package. 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.

Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.

Skills Desired

Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives.

Global Program Regulatory Director employer: GB16 (FCRS = GB016) Novartis Pharmaceuticals UK Ltd.

At Novartis Pharmaceuticals UK Ltd., we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration. Our commitment to employee growth is evident through continuous learning opportunities and the chance to work on groundbreaking projects in medical analytics and AI. Located in a vibrant area, our team enjoys a supportive environment that values diversity and encourages meaningful contributions to drug development.

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Contact Details:

GB16 (FCRS = GB016) Novartis Pharmaceuticals UK Ltd. Recruitment Team

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We think you need these skills to ace Global Program Regulatory Director

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