Senior Regulatory Affairs Group Director, Late CVRM
Are you passionate about science and experienced within regulatory affairs and drug development? Do you possess strategic and operational leadership skills? Then, join us at Cardiovascular, Renal or Metabolism (CVRM) regulatory affairs to get involved in the global regulatory strategies and support the research, development and commercialization of our products across the portfolio!
AstraZeneca’s pipeline of innovative medicines is consistently growing within Cardiovascular, Renal and Metabolism (CVRM). Within CVRM Regulatory Affairs we take innovative regulatory approaches to bring these CVRM life-changing treatments to those who need it – working across our early and late-stage development pipeline and the business as efficiently and effectively as possible. As an industry leading CVRM Regulatory function, we’re focused and committed to the development of our products as well as to our people – providing an open and supportive space to explore, learn and develop across all regulatory roles and levels.
We are seeking a dynamic and experienced Senior Regulatory Affairs Group Director (SrRAGD) to join the Regulatory Affairs Management (RAM) group supporting the CVRM Therapeutic Areas. In this role, you will play a pivotal role in developing and shaping the strategic direction of the group, ensuring improved efficiency, performance, and quality of the RAM community. You will also be part of leading and developing the broader Late CVRM Regulatory team, driving our vision of being an industry-leading regulatory organization and a great place to work.
What You'll Do
Provide leadership, coaching and line management for a group of Regulatory Affairs Managers based in Boston and Mississauga
Ensure efficient, targeted recruitment for the group and lead talent and performance development activities
Collaborate with the RAM leadership team to set the strategy for tactical delivery and efficiency for drug projects
Drive improvement projects and embed change in the organization
Establish and develop relationships with key stakeholders, internally and externally
Essential For the Role
Bachelors Degree in Science or related discipline
10+ years’ experience in regulatory affairs in the pharmaceutical industry or at a health authority
Knowledge of regulatory procedures and legislation for drug development throughout the product lifecycle
Extensive experience in managing people and organisations in a matrixed organizational structure
Excellent collaboration, team working, oral and written communication skills
At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering groundbreaking methods and bringing unexpected teams together. Interested? Come and join our journey.
We are eager to know more about you. If you are interested to know more about us, apply now!
As AstraZeneca continues to put patients at the forefront of our mission, we are excited for our move to Kendall Square/Cambridge in 2026. Find out more information here:
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
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