Executive Regulatory Science & Strategy Director, Oncology

Within Oncology Regulatory Affairs, we work in areas of unmet need and take innovative regulatory approaches to bring life‑changing treatments to those who need it – working across our pipeline and the business to get medicines to patients as efficiently and optimally as possible. As an industry leading Oncology Regulatory function, we’re growing fast, and we’re as passionate about and committed to the development of our people as we are our business – providing an open and encouraging space to explore, learn, grow and develop across all roles and levels. At AstraZeneca, we share and are motivated by the same purpose: pushing the boundaries of science in order to deliver life‑changing medicines to patients around the world. Everything we do is underpinned by our dedication to being a phenomenal Place to Work. We recognize that our people are our greatest asset and know what’s possible with an accomplished and diverse team that believes in what science can do. We are more than 65,000 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 limitless world of science through our remarkable product pipeline, and we take our understanding of many therapeutic areas to a whole new level by seeking new treatments. The Executive Regulatory Science Director is a role that provides global strategic regulatory expertise and oversight to support the research, development and commercialization of products across both small molecules and biologics. The position that is currently being recruited is within the Oncology therapy area and specifically leading the Oncology Breast Cancer group. How you will make a difference Coach and mentor regional (US and EU regulatory leads) and global regulatory leads, including identification of skill development opportunities for regulatory professionals with different levels of experience. Partner with Regulatory Affairs Directors aligning on global innovative regulatory strategies for products. Lead resource planning and recruitment of staff. Provide critical review and input on disease area and portfolio regulatory strategies, risk planning and mitigations. Represent the Global Regulatory Affairs function in senior level interactions at internal governance technical review committees, key global health authority meetings and external partners. Collaborate with regional policy and intelligence groups to critically analyze emerging science, data and changes in the regulatory environment and advise senior management on project risks/mitigation activities accordingly. Define and drive disease area global regulatory policies and priorities. Review and approve high‑level documents for global regulatory submissions as well as core prescribing information. Ensure submission excellence framework is timely and consistently applied across projects including sharing best submission practices and knowledge and using existing tools. Sponsor key non‑drug project workstreams, business initiatives, external activities and meetings and act as a subject‑matter expert. What You'll Need Bachelor’s degree in life sciences and/or science related field and/or other appropriate knowledge/experience. MSc, PhD, PharmD, MD is a definite asset. More than 10 years drug development experience. Oncology therapy area knowledge/experience, ideally expertise with breast tumor types. Deep knowledge of global regulatory strategy experience with all phases of oncology drug development, including early drug development as well as direct involvement in marketing applications that have progressed through to registration. Significant experience in leading major health authority interactions. Proven experience of growing high‑performance teams, attracting top talent and developing capabilities of regional and global regulatory leads. Experience in leading people in a matrixed interpersonal structure. Ability to think strategically and critically to evaluate risks to regulatory product development and approval, market entry and licence maintenance activities. Ability to travel domestically and internationally. Competitive salary and benefits package on offer The annual base salary in the US ranges from $276,000 to $414,000. Base pay may vary depending on market location, job‑related knowledge, skills and experience. In addition, positions offer a short‑term incentive bonus opportunity, eligibility to participate in our equity‑based long‑term incentive program (salaried roles) or a retirement contribution (hourly roles). Benefits include a qualified retirement program (401(k) plan), paid vacation and holidays, paid leaves and health benefits including medical, prescription drug, dental and vision coverage. If hired, the employee will be in an at‑will position and the Company reserves the right to modify base salary or other compensation at any time. Our mission We are committed to creating an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form. #J-18808-Ljbffr