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!
Check you match the skill requirements for this role, as well as associated experience, then apply with your CV below.
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 more than 90,000 people in over 100 countries. Our aim is simple : to positively impact lives together. Using the power of science and innovation, our people improve the impact medicine has on patients.
Together, we explore the world of science through our remarkable product pipeline and we take our understanding of the CVRM therapeutic area to a whole new level by seeking new treatments.
We continue to expand our regulatory teams at AstraZeneca’s dynamic R&D sites in Gaithersburg (US) and Boston, MA (US). If you are looking for a new challenge, we are offering opportunities in different disease areas and at different levels, depending on your expertise and previous experience.
What You’ll do
As a Regulatory Affairs professional within AstraZeneca, you will play a key role in channeling our scientific capabilities to make a positive impact on changing patients’ lives.
In Regulatory Affairs, our teams influence the development of our innovative pipeline, define the regulatory strategy for our therapeutic assets, and engage with Health Authorities to effectively inform our development programs.
In this way, our Regulatory Affairs teams are transforming exciting science into valued new medicines for patients around the world.
Strategic thinking is key within our function. The more experienced you are, the more accountability you will have for strategic leadership including responsibility for development and implementation of the global regulatory strategy for a product / group of products of increasing complexity.
Essential for the role
- Bachelors degree in a science related field.
- 3+ years of proven experience defining and implementing the regulatory strategy for a pharmaceutical organization.
- Extensive knowledge of regulatory affairs within one or more therapeutic areas in early and late development.
- Proven track record of regulatory drug development including product approval / launch.
- Experience in leading Major Health Authority interactions.
- Ability to think strategically and critically and evaluate risks to regulatory activities.
- Ability to work strategically within a complex, business-critical and high-profile development program.
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.
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