Key Responsibilities

• Drive continuous improvement of global regulatory processes supporting clinical trial applications across multiple regions.
• Lead process design, optimisation and implementation initiatives to enhance quality, compliance and operational efficiency.
• Partner with cross-functional stakeholders to identify process gaps and deliver sustainable solutions.
• Monitor regulatory process performance and recommend data-driven improvements to accelerate execution.
• Develop and maintain process documentation, standards and governance frameworks across the organisation.
• Support digital transformation initiatives by embedding innovative tools and best practices into workflows.
• Champion change management activities to ensure successful adoption of new processes and ways of working.

Essential Requirements

• Bachelor's degree in life sciences, pharmacy, healthcare or a related scientific discipline.
• Significant experience in regulatory affairs, clinical development or pharmaceutical process management.
• Strong understanding of global clinical trial regulations and regulatory submission processes.
• Proven ability to lead complex process improvement and transformation initiatives across global organisations.
• Excellent stakeholder management skills with experience influencing diverse cross-functional teams.
• Strong analytical, problem-solving and project management capabilities with a focus on delivering measurable outcomes.

Benefits & Rewards

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.

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.

Read our brochure to learn more about our global total rewards offering:

https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf

• Drive continuous improvement of global regulatory processes supporting clinical trial applications across multiple regions.
• Lead process design, optimisation and implementation initiatives to enhance quality, compliance and operational efficiency.
• Partner with cross-functional stakeholders to identify process gaps and deliver sustainable solutions.
• Monitor regulatory process performance and recommend data-driven improvements to accelerate execution.
• Develop and maintain process documentation, standards and governance frameworks across the organisation.
• Support digital transformation initiatives by embedding innovative tools and best practices into workflows.
• Champion change management activities to ensure successful adoption of new processes and ways of working.

• Strong understanding of global clinical trial regulations and regulatory submission processes.
• Excellent stakeholder management skills with experience influencing diverse cross-functional teams.
• Strong analytical and problem-solving capabilities.
• Project management capabilities with a focus on delivering measurable outcomes.
• Ability to lead complex process improvement and transformation initiatives across global organisations.

• Bachelor's degree in life sciences, pharmacy, healthcare or a related scientific discipline.
• Significant experience in regulatory affairs, clinical development or pharmaceutical process management.