Senior Manager, Regulatory Affairs US Lead

Alexion Pharmaceuticals, Inc.; Boston (MA); On-site; USD 136,000 - 203,000; Full time

Benefits offered by this job

Incentives

Benefits package

Job summary

Alexion Pharmaceuticals, Inc. in Boston seeks a Senior Manager, Regulatory Affairs US to lead regulatory strategies and submissions for assigned products, enabling lifecycle management and timely approvals.

The role emphasizes collaboration with cross-functional teams, FDA interactions, and keeping current with evolving regulations to support rare-disease therapies.

Qualifications

• 6+ years of regulatory experience in pharma, US-focused.
• Bachelor’s degree in life science; graduate degree preferred.
• Experience providing strategic regulatory advice for global development.
• Ability to manage multiple projects in time-sensitive timelines.
• Strong collaboration across global teams and Senior Management.
• Excellent communication and presentation skills.
• Familiarity with new regulations and GxP understanding.

Responsibilities

• Develop and implement US regulatory strategies for assigned projects.
• Manage US regulatory submissions (INDs, BLAs/NDAs, pediatric submissions, etc.).
• Represent Alexion as the point of contact with the US FDA and coordinate meetings.
• Oversee regulatory authorizations in the assigned jurisdiction.
• Collaborate with Regulatory, Commercial, Medical, and cross-functional teams.
• Stay up-to-date on latest regulatory requirements and trends.

Skills

Regulatory strategy

US regulatory

Submissions management

Cross-functional leadership

Project management

Communication skills

Education

Bachelor’s degree in life science

Postgraduate degree (MSc, PharmD, or PhD) preferred

Tools

Veeva

Microsoft 365

Job description

Location: Seaport, Boston or Gaithersburg, Maryland

Reports to: Senior Director, Global Regulatory Strategy

About Alexion

For over 30 years, Alexion has been dedicated to transforming the lives of people living with rare diseases. We lead with breakthrough science, deep disease understanding, and a dedicated commitment to patients. As part of AstraZeneca, we are uniquely positioned to accelerate innovation and reach more patients globally.

Working here means being driven by purpose, acting with integrity, and fostering a culture where people feel valued, connected, and empowered. You'll join a community that puts patients first, plays to win, and supports your development at every step.

Role Overview

The Senior Manager, Regulatory Affairs US lead will be responsible for leading, planning, preparing and delivering regulatory strategies and activities for assigned product(s)/project(s) across the assigned jurisdiction supporting global regulatory strategies, with the intention of achieving successful registration and lifecycle management of unique and technologically complex products serving patients with rare diseases and unmet medical needs.

This individual will provide tactical and strategic regulatory input and leadership across regulatory and cross-functional teams, 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.

Key Responsibilities

• Accountable as US Regulatory Lead to develop and implement regulatory strategies for assigned project(s)/product(s) in the US and accountable to provide regulatory advice to cross-functional strategies and associated deliverables according to business objectives.
• Responsible for the management and execution of regulatory submissions in the US (e.g. INDs, BLAs/NDAs, orphan drug designation applications, pediatric submissions, etc.), by actively collaborating with other Regulatory functions and cross-functional teams to deliver business objectives for assigned products/programs..
• Represents Alexion as point of contact with the US FDA or other relevant external partners, including the planning and management of regulatory authority meetings, in alignment with global regulatory and cross-functional strategy.
• Responsible for overseeing operational activities related to the Regulatory authorizations according to current regulatory internal and external requirements for the assigned jurisdiction(s).
• Supports the Global Regulatory Lead in internal Governance and advisory bodies, or other relevant internal activities, including the development and management of select Regulatory processes and procedures, as well as inspection/audit support.
• Actively collaborates with other Regulatory teams and Enterprise functions (e.g. Commercial, Medical) to provide regulatory input to business-relevant deliverables concerning assigned project/product and jurisdiction.
• Actively be up to date on and efficiently apply latest regulatory requirements and trends, within assigned jurisdiction and regulatory focus area (e.g. clinical development, lifecycle management).
• Ensure exemplary behavior, leadership, ethics and visibility within the Enterprise, with Health Authorities and other external partners.

You Will Need To Have

Qualifications & Education

• 6+ years of relevant Regulatory experience in the pharmaceutical industry, with experience in US regional regulatory strategies.
• Bachelor’s degree in life science required; relevant postgraduate degree (e.g., MSc, PharmD, or PhD) is preferred.
• Experience providing strategic regulatory advice in relevant regulatory jurisdiction(s) (e.g., US) for the global development of products through all stages of development including pre-approval and marketed assets.
• Ability to run 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, including Senior Management.
• Strong interpersonal, written/verbal communication and presentation skills. Consistent track record practicing sound judgment as it relates to risk assessment.
• 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.

Competences

• Excellent use of Microsoft 365 (Office) tools, ideally well skilled on the use of PowerPoint
• Experience working in a regulatory documentation system (like Veeva).
• Proficient in English in the Corporate setting. Additional languages desirable.

Why Alexion?

At Alexion (AstraZeneca’s Rare Disease unit), work centres on people living with rare conditions whose journeys demand new thinking every day; this means operating at the edge of science while staying grounded in real patient stories, collaborating across subject areas to turn complex biology into transformative medicines, learning fast in an entrepreneurial environment with the backing of a global biopharma, and growing through tailored development that deepens both leadership capability and compassion for patients and communities we serve.

If this opportunity to redefine what patient engagement can be resonates,

Benefits

• The annual base pay for this position ranges from $135,624.80 - $203,437.20 USD Annual. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Our mission is to build 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 their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.