This position supports cross-functional development teams for innovative drug development at any stage of development - from research throughout clinical development until MAA, NDA/BLA. Responsibilities: Provide strategic regulatory guidance to project teams Cover clinical development in the project teams Plan and execute client's the global regulatory development plan Responsible for the global agency interaction strategy Requirements: Msc in Life Sciences, Medicine or Animal medicine Around 10 years in clinical regulatory affairs Practical experience in strategic clinical development (not clinical operations) Strategic thinker, solution-oriented Ability to work independently and manage multiple tasks simultaneously