Senior Regulatory Affairs Director (Cardiovascular, Renal & Metabolism)

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Lead the Regulatory Vision for projects in AstraZeneca CVRM's exciting portfolio
Are you a seasoned regulatory strategist ready to shape the future of Regulatory while guiding innovative medicines from development through to patients worldwide? Join AstraZeneca's Cardiovascular, Renal & Metabolism (CVRM) team as a Senior Regulatory Affairs Director and become a recognized leader who drives regulatory excellence within our function and across the broader regulatory community.

About AstraZeneca
At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big, and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.

About the Role
As aSenior Regulatory Affairs Director, you'll lead the regulatory strategy for large and complex drug development projects or programs/franchises spanning multiple indications asGlobal Regulatory Lead (GRL), Franchise GRL, or in a dual role as GRL and Regional Regulatory Lead.In your role as a Senior RAD you will also contribute to shaping the future of our Regulatory function through mentorship, innovation, and external thought leadership.

This senior role distinguishes itself through:
•Franchise-level leadershipacross multiple indications and development programs (vs. single project/indication focus)

•Dual capacityto serve as both GRL and Regional Lead as required

•Mentorship and coaching responsibilityfor developing regulatory talent and building team capabilities

•External thought leadershipestablishing you as a recognized voice in the regulatory community

•Functional innovationdriving the development of novel regulatory tools, technologies, and approaches

Strategic Leadership at Scale
•Lead the development and implementationof the global regulatory strategy for complex projects or franchises with multiple indications and development programs, ensuring rapid approval with competitive labeling that meets patient, market, and business needs

•Lead the Global Regulatory Strategy Team (GRST)which may include other GRLs responsible for specific indications, and experts across regions and Regulatory skill groups

•Represent Regulatory Affairson Global Product Teams (GPTs) or Franchise leadership teams, providing strategic regulatory counsel that shapes overall product and clinical strategy

•Serve as a thought leaderat industry conferences, regulatory forums, and trade organizations, representing AstraZeneca's regulatory excellence externally

Foster a cultureof strategic thinking, innovation, and regulatory excellence

Essential Experience & Qualifications
•Advanced degreein a science-related field and/or equivalent knowledge/experience

•7-10 yearsof regulatory drug development experience including product approval and launch

•Proven track recordof leading at least one major regulatory approval at a global level, including response team leadership and labeling negotiations

•Extensive experienceleading major Health Authority interactions

•Deep knowledgeof regulatory affairs spanning both early and late development in one or more therapeutic area(s)

•Demonstrated leadershipin complex, business-critical, high-profile development programs

Essential Skills & Competencies
•Strategic thinkingwith the ability to critically evaluate risks and opportunities across a franchise

•Strong influencing skillswith proven ability to drive alignment at senior levels both internally and externally

•Excellent communicationabilities, both written and oral, with confidence presenting to executive leadership, regulatory agencies, and external audiences

•Innovation mindsetwith initiative to challenge conventional approaches and drive functional advancement

•Mentorship capabilitywith track record of developing regulatory talent

Why AstraZeneca?
At AstraZeneca, we're dedicated to being a Great Place to Work. You'll be empowered to push the boundaries of science and unleash your entrepreneurial spirit. We offer:

•Impact: Direct influence on medicines that change patient lives

•Collaboration: An inclusive culture that champions diversity and values Regulatory Affairs as an equal partner

•Growth: Commitment to lifelong learning and career development

•Innovation: Work on a rich and diverse pipeline of both small and large molecules

•Flexibility: Individualized ways of working that balance personal and professional commitments (3 days per week in office)

There's no better place to make a difference to medicine, patients, and society. Join us on our exciting journey to pioneer the future of healthcare.

Date Posted
02-Apr-2026
Closing Date
29-Apr-2026Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.