Regulatory Affairs Manager

AstraZeneca plc; Camden Town; On-site; GBP 70,000 - 110,000; Full time

Job summary

AstraZeneca plc in Pancras Square, London, is seeking an experienced Regulatory Affairs professional to deliver and maintain competitive UK licences, drive regulatory strategy for new initiatives, and ensure compliance with GRP and the local QMS.

You will lead UK submissions, collaborate with cross-functional teams, engage with the MHRA, and support investigational and in-licensed products across the product lifecycle, ensuring timely approvals and robust regulatory governance.

Qualifications

• 4+ years in a regulatory affairs role within a pharma company.
• Post-Brexit UK regulatory experience.
• Ability to lead cross-functional interactions and negotiate effectively.

Responsibilities

• Generate and maintain UK regulatory licences.
• Regulatory governance and compliance delivery.
• Provide regulatory strategy leadership across projects.
• Lead the organisation and improve productivity.
• Support submissions and clinical regulatory activities (e.g., CMC, labeling).
• Coordinate with MHRA and external stakeholders.

Skills

Regulatory affairs

UK regulatory experience

Cross-functional coordination

Negotiation skills

Lifecycle license management

Regulatory strategy

IT systems proficiency

Audit & inspection knowledge

Education

Life sciences degree

Professional qualifications

Tools

Veeva systems

Job description

Type: Permanent

Location: Pancras Square

Introduction to the role

Deliver and maintain competitive licences for the UK, driving regulatory strategy for new initiatives and ensuring regulatory compliance for defined product and project responsibilities, including project leadership. Achieve timely delivery of clinical trial approvals and maintain high regulatory compliance standards for the UK through the provision of local regulatory expertise. Support the development of AstraZeneca investigational and in-licensed/co-development products through valued contributions to cross-functional projects, study feasibility questionnaires, scientific advice meetings, and other related activities. Ensure full compliance with GRP requirements in line with the local Quality Management System (QMS) SOP and all other AstraZeneca policies and standards.

Accountabilities

• Generate Competitive Licences (0-40%)
• Regulatory Compliance & Governance (0-10%)
• Commercial Support (0-15%)
• Formulate and Influence Regulatory Strategy (0-15%)
• Lead the Organisation and Improve Productivity (0-10%)
• Clinical Support (0-10%)

Essential Skills/Experience

• Life sciences degree or appropriate professional qualifications.
• 4+ years’ experience working within a regulatory affairs organisation in a UK-based or global pharmaceutical company.
• Post-Brexit UK regulatory experience.
• Business relationship management skills and the ability to navigate and coordinate cross-functional interactions..
• Operational regulatory experience in the pharmaceutical industry with time spent in a commercially aware role
• Demonstrable negotiation skills.
• Ability to make optimal use of IT systems.
• Knowledge of the external regulatory environment and regulatory science expertise support building a productive, positive and trustworthy relationship with the UK MHRA to drive meaningful interactions to the benefit of patients.
• Lifecycle maintenance of UK Regulatory licenses, including different types of submissions, including but not limited to CMC, Labelling, etc.
• Optimisation and continuous improvement of submissions throughout the product lifecycle, applying global quality standards and timelines.
• Development of regulatory strategy aligned with the disease area strategy/target product profiles, providing sustainable competitive advantage in alignment with product development and commercialisation strategies.
• Application of knowledge of changing regulatory environments to ensure compliance, minimise risk and create business opportunities.
• Application of drug development knowledge.
• Audit and inspection knowledge.

Desirable Skills/Experience

• Experience with clinical trial applications and trial maintenance activities, including the use of in-vitro diagnostics (IVDs) in the clinical trial setting.
• Experience using AI solutions to simplify and improve departmental processes/ways of working.
• Experience in creating and delivering regulatory strategies for marketing authorisation applications and new indications.
• Experience working in Veeva systems.
• Management of reactions to change while remaining effective in new work situations and times of uncertainty; assessment, planning and management of the impact of changes on stakeholders; and application of change management techniques to engage stakeholders appropriately.
• A robust understanding of a relevant disease and therapeutic area, including the regulatory and health technology assessment environment in the major markets, the competitor landscape, and predictable barriers/obstacles in development.

At AstraZeneca, we change the practice of medicine by generating compelling medical evidence that helps physicians better treat patients at every point in their journey. Our cross-functional teams work seamlessly together, leveraging diverse skills to advance our pipeline and redefine cancer treatment. We foster a culture of openness, transparency, ambition, and drive. Here, you will find a supportive environment where you can grow your career while making a significant impact on patients' lives.

Date Posted

26-Oct-2026

Closing Date

09-Nov-2026Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.