.Location: Barcelona, SpainWould you like to use your Regulatory Intelligence skills to ultimately help get Oncology medicines to patients that need them? If you would, please read on...At AstraZeneca, work with a diverse set of minds, all united by a shared passion to learn, grow, and discover. Within Oncology Regulatory Science and Strategy (ORSS), we bring hope and solutions to patients with unmet needs across the globe. As Regulatory professionals working on Oncology products, we work in areas of unmet need and take innovative regulatory approaches to bring life-changing treatments to patients.We work across our pipeline and the business to get medicines to patients as efficiently and effectively as possible. The Regulatory Intelligence Director (RID) - Oncology is responsible for providing global therapeutic area-specific Regulatory interpretation and impact analysis of emerging competitive intelligence. This role will work closely with other Intelligence groups within AZ (Global Regulatory Policy & Intelligence (GRPI), Clinical Information Science, and Global Insights, Analytics, and Commercial Excellence (GIACE)). The RID will work closely with Therapeutic Area (TA) VP, Executive Regulatory Science Directors, Global Regulatory Leaders (GRLs), and Regulatory Affairs Directors (RADs) to provide the Regulatory Intelligence aspect of disease areas and product-specific Regulatory strategies.You will liaise with GRPI on Regulatory policy matters and lead a coordinated response in providing feedback by obtaining input from key experts and partners in the therapeutic area. The RID will liaise with International, China, and Japan RADs regarding therapeutic area-specific guidance and regulatory intelligence aspects in each region, contributing to overall Regulatory landscape per disease/scientific platform. You'll be responsible for communicating the Regulatory impact and implications of relevant competitive intelligence within therapeutic area and across the organization as appropriate.Typical Accountabilities, what you will be doing:Conduct analysis and impact assessment of Regulatory Intelligence across the portfolio in a given therapeutic area (TA) and communicate findings to key partners and senior leaders within the therapeutic area.Work closely with other Intelligence groups within the company (GRPI, GIACE, Clinical Information Science, etc.) to provide the disease area/scientific platform specific Regulatory interpretation and impact.Serve as the central point person within TA in leading tailored Regulatory research for RADs including project level Regulatory strategy, due diligence, disease area strategy, initiatives etc
