Key Responsibilities

• Lead and develop a global regulatory team delivering high-quality, compliant and timely clinical trial submissions and approvals.
• Coach and support team members, building capability and enabling professional growth.
• Allocate resources effectively across the assigned portfolio, balancing priorities and business needs.
• Drive process improvement, simplification and automation to strengthen operational excellence.
• Build strong, customer-focused relationships with key stakeholders and act on feedback.
• Foster collaboration and knowledge sharing across Regulatory Affairs and global teams.
• Champion change and role-model Novartis culture, values and behaviours.

Essential Requirements

• Bachelor’s or Master’s degree in a science-related discipline, with relevant regulatory experience and demonstrated capability.
• Substantial knowledge and experience of global regulations, guidelines and processes supporting regulatory clinical trial activities.
• Demonstrated experience leading regulatory professionals, with strong people management, coaching and development capabilities.
• Strong experience in strategic planning, regulatory review, compliance, submissions and execution.
• Demonstrated ability to drive process improvement, simplification, automation and operational excellence.
• Strong communication, influencing and problem-solving skills within complex, cross-functional and international environments.

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.

Commitment to Diversity and Inclusion / EEO paragraph

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

• Lead and develop a global regulatory team delivering high-quality, compliant and timely clinical trial submissions and approvals.
• Coach and support team members, building capability and enabling professional growth.
• Allocate resources effectively across the assigned portfolio, balancing priorities and business needs.
• Drive process improvement, simplification and automation to strengthen operational excellence.
• Build strong, customer-focused relationships with key stakeholders and act on feedback.
• Foster collaboration and knowledge sharing across Regulatory Affairs and global teams.
• Champion change and role-model Novartis culture, values and behaviours.

• People management, coaching and development
• Strategic planning
• Regulatory review, compliance, submissions and execution
• Process improvement, simplification, automation and operational excellence
• Communication, influencing and problem-solving
• Working within complex, cross-functional and international environments

• Bachelor’s or Master’s degree in a science-related discipline
• Relevant regulatory experience and demonstrated capability
• Substantial knowledge and experience of global regulations, guidelines and processes supporting regulatory clinical trial activities
• Demonstrated experience leading regulatory professionals