As a Regulatory Affairs professional within Organization, 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.
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
Organization 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 straightforward to positively impact lives together. Using the power of science and innovation,