Global Regulatory Director, RA Central Solutions CTA/CTR

C028 (FCRS = CH028) Novartis Pharma AG; Basel-Stadt; Hybrid; CHF 142,000 - 264,000; Full time

Job summary

Novartis Pharma AG in Basel, Switzerland, seeks a Global Regulatory Director - RA Central Solutions to lead global regulatory submissions for clinical trials and to build a high-performing team across functions. The role emphasizes coaching, resource alignment and strategic influence to accelerate compliant approvals and drive innovation.

You will shape regulatory strategy, drive excellence through automation, and collaborate with senior stakeholders to advance Novartis’ portfolio in a

Qualifications

• Significant experience leading global clinical trial applications across international markets.
• Deep understanding of worldwide regulatory requirements and submission processes for clinical trials.
• Ability to coach and develop diverse, cross-cultural teams while fostering high performance.
• Experience driving operational excellence, process improvement and automation initiatives.

Responsibilities

• Lead global clinical trial application activities and ensure compliant submissions worldwide.
• Build and inspire a high-performing regulatory team through coaching and mentoring.
• Allocate resources to meet clinical trial milestones across the portfolio.
• Drive process simplification and automation to improve operations.
• Partner with senior stakeholders to shape regulatory strategy and priorities.
• Foster cross-functional collaboration and a customer-focused culture within Regulatory Affairs.

Skills

Global regulatory leadership

Clinical trial submissions

Team development

Process improvement

Cross-functional collaboration

Regulatory strategy

Job description

Salary Range: CHF142,100.00 - CHF263,900.00

Job Description Summary #LI-Hybrid Location: Basel, Switzerland

Relocation Support: This role is based in Basel, Switzerland. Novartis is unable to offer relocation support.

What if you could shape the future of global clinical trial execution while leading a high-performing team at the forefront of regulatory innovation? As Global Regulatory Director - RA Central Solutions, you will play a pivotal role in ensuring timely, compliant clinical trial applications across a diverse global portfolio. You'll empower and develop talented regulatory professionals, drive operational excellence through process simplification and automation, and influence strategic decisions that strengthen Novartis' ability to bring innovative medicines to patients worldwide. This is an exciting opportunity to lead meaningful change, build strong cross-functional partnerships, and help create a more agile, future-ready Regulatory Affairs organisation.

Job Description Key Responsibilities

• Lead global clinical trial application activities, ensuring high-quality, compliant submissions and approvals worldwide in collaboration with RA DU Lead.
• Build, develop and inspire a high-performing regulatory team through coaching, mentoring and talent development.
• Allocate resources strategically to deliver clinical trial milestones efficiently across the assigned portfolio.
• Drive process simplification, automation and continuous improvement to enhance operational excellence.
• Partner with senior stakeholders to shape strategy and support key regulatory business priorities.
• Foster strong cross-functional collaboration and a customer-focused culture across Regulatory Affairs.
• Champion organisational change, promoting Novartis values, innovation and knowledge-sharing across teams.

Essential Requirements

• Significant experience leading global clinical trial application and registration activities across international markets.
• Deep understanding of worldwide regulatory requirements, guidelines and submission processes for clinical trials.
• Ability to lead and develop diverse, cross-cultural teams, with a demonstrated ability to coach, mentor and grow talent while fostering an inclusive, high-performing environment.
• Strong experience driving operational excellence, process improvement and automation initiatives.
• Demonstrated ability to influence stakeholders and lead change across cross-functional organisations.
• Excellent communication, problem-solving and strategic planning skills with a strong focus on delivering results.

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: CHF142,100 to CHF263,900 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. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Long-term equity awards granted at group level may also be part of your package. Further details will be provided during the application process. 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.

Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf 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 / EEO Paragraph

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

Accessibility and Accommodation

Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need reasonable accommodation for any part of the recruitment process, or to receive more detailed information about the essential functions of a position, please send an e-mail to [e-mail] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

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.