You will lead the design and execution of the global medical strategy for highly specialized assets with significant unmet medical need. You will play a key role in shaping the clinical and scientific narrative, enabling evidence generation, and building
Responsible for driving awareness and implementation of data standards and associated best practices in systems to support Regulatory Requirements for data submissions and to enable Regulatory data to connect with data sourced from other functions
Act as the Safety Science representative in the Medical Development Team (MDT) and ensure integration of safety into product development and lifecycle decisions; Provide clinical safety input into study design, conduct, analysis and interpretation,
This role will involve designing and overseeing experimental studies, analysing results, and generating high-quality data packages and presentations to support internal decision making and customer engagement. The successful candidate will work closely