This is what you will do:

TheRegulatory Affairs Director (RAD), Regulatory Science & Execution will be accountable for the development, implementation and maintenance ofregulatory strategies for assigned project(s)/product(s) and regulatory jurisdiction(s), with the intention of achievingsuccessful registration and lifecycle management of unique and technologically complex products serving patients with rare diseases and unmet medical needs.

This individual willprovide tactical and strategic input to and leadership acrossregulatory and cross-functional teams with the objective of delivering according to regional and global Business Objectives. The individual will also ensure effective communication and constructive working relationships with business partners and representatives of regulatory authorities.

You will be responsible for:

Accountable as Regulatory Lead to develop and implement regulatory strategies for assigned highly complex project(s)/product(s) across the assigned jurisdiction(s) and accountable to provide regulatory advice to cross-functional strategies and associated deliverables according to business objectives with limited oversight.

Accountable for the regulatory execution of submissions in the relevant regulatory jurisdiction(s), by actively collaborating with other Regulatory functions and cross-functional teams (e.g. clinical trial applications, marketing authorization applications, orphan drug designation applications, paediatric submissions, etc.).

Leads the planning and conduct of regulatory authority meetings in relevant jurisdiction(s), in alignment with global regulatory and cross-functional strategy. Represents Alexion as point contact with relevant Health Authorities and/or lead interactions with such authorities or other relevant external stakeholders.

Actively collaborate with Senior Management and Enterprise functions (e.g. Clinical, Commercial, Medical Affairs, amongst others) to provide regional regulatory insight and broader drug development expertise.

Actively be up to date on latest regulatory requirements and trends, and contribute to the shaping of the regulatory science environment. Support regulatory intelligence and policy priorities based on Alexion and AstraZeneca’s internal knowledge and expertise. Champion opportunities for regulatory innovation approaches and present such strategies and plans to management and appropriate cross-functional teams.

Supports relevant internal activities, including development and management of select Regulatory processes and procedures, as well as inspection/audit support.

Demonstrate strategic leadership skills contributing to effective product development. Provide team leadership and participate in mentoring, and performance feedback to regulatory and cross-functional colleagues.

Ensure exemplary behavior, leadership, ethics and transparency within the Enterprise, with Health Authorities and other external stakeholders.

You will need to have:

8+ years of relevant Regulatory experience in the pharmaceutical industry, with experience in US regional regulatory strategies.

Bachelor's Degree

Strong knowledge of drug development and regulatory environment, coupled by excellent scientific and business judgment.

Experience providing strategic regulatory advice in several regulatory jurisdiction(s) (e.g. EU, US, Canada, UK) for the global development of products through all stages of development including pre-approval and marketed assets.

Ability to manage complex issues and lead multiple projects simultaneously in a time-sensitive fashion.

Ability to build intra- and inter-team relationships and collaborate in a global team environment at all levels of the organization, especially Senior Management.

Strong interpersonal, written/verbal communication and presentation skills.

Proven track record practicing sound judgment as it relates to risk assessment

Highly familiar and knowledgeable of new and emerging regulations and guidances. Understanding of GxPs at relevant areas and solid understanding of where to seek and how to interpret regulatory information.

The annual base pay for this position ranges from $173,600.80 - $260,401.20. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.