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 innovative science.
- Benefits: Competitive salary, performance bonuses, flexible working, and comprehensive benefits package.
- 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: Advanced degree in a scientific discipline and significant regulatory affairs experience required.
The predicted salary is between 83510 - 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.
About The Role
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
At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. Expected Annual Base Salary Range for role: £83,510 to £155,090. 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. Long-term equity awards granted at group level may also be part of your package. Further details will be provided during the application process. 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.
Commitment to Diversity and Inclusion / EEO
Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.
Why Novartis
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. Ready to create a brighter future together?
Global Program Regulatory Director 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. As a Global Financial Controls & Compliance Process Experts Senior Manager, you will benefit from competitive compensation, flexible working options, and a commitment to employee growth through continuous learning and development opportunities. Join us in shaping the future of healthcare while enjoying a diverse and inclusive environment that values your contributions and well-being.
StudySmarter Expert Advice🤫
We think this is how you could land Global Program Regulatory Director
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We think you need these skills to ace Global Program Regulatory Director
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 Novartis UK!
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How to prepare for a job interview at Novartis UK
✨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 Novartis UK that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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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.
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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.
