Regulatory Affairs Manager

Astrazeneca

Regulatory Affairs Manager Introduction to role Are you ready to lead regulatory submissions that accelerate access to life-changing medicines? Do you thrive in a dynamic setting where your judgment shapes approval pathways and your work directly impacts patients in need? As a Regulatory Affairs Manager, you will own end-to-end planning, coordination and delivery of regulatory submissions across regions and modalities, translating scientific strategy into high-quality applications that secure timely approvals. You will identify risks and opportunities, advise cross-functional teams on procedural and documentation requirements, and guide products through development, authorization and lifecycle management. This role places you at the heart of a science-led organization focused on getting the right medicines to the right patients, faster than ever before. You will work with diverse teams, influence submission strategy, and help set the standard for how we partner with Health Authorities to achieve rapid, global approvals. Accountabilities Regulatory Strategy and Planning: Understand the regulatory framework and regional trends for small and large molecules across all regions, informing submission strategy and procedural choices to maximize speed and quality of approvals. Submission Leadership: Lead and contribute to planning, preparation (including authoring where relevant) and delivery of simple and, with experience, increasingly complex submissions throughout the product lifecycle from global and/or regional perspectives; connect immediate deliverables to future label and lifecycle opportunities. Procedural and Documentation Guidance: Provide regulatory input on Health Authority requirements for assigned deliverables, including submission delivery strategy per market/region, review of documents (e.g., response documents, study protocols, PSRs), and analysis of regulatory procedures and special designations used during development, authorization and extension. Best Practices and Health Authority Engagement: Use and share best practices when handling various applications and procedures during interactions with Health Authorities and in day-to-day work, operating effectively in a highly dynamic environment to drive confident, consistent outcomes. Integrated Project Management: Develop, execute and maintain submission delivery plans and content plans; proactively provide status updates to stakeholders; coordinate input, maintenance and revisions in Planit project plans; highlight unforeseen changes in resource demand to the Lead RPM and line manager. Risk Management: Identify regulatory risks early and propose clear mitigations to the Lead RPM and cross-functional teams, protecting timelines and the quality of submissions. Operational Excellence and Compliance: Support operational and compliance activities for assigned deliverables, including generating work requests and submission content plans, submission tracking, TMF and document management, collaborating with GRO, Markets, CROs and alliance partners where relevant. Cross-Functional Collaboration and Influence: Provide regulatory expertise and guidance to cross-functional teams, working flexibly across regions to ensure business objectives are met and strategic value is realized. Coaching and Knowledge Sharing: Provide coaching, mentoring and knowledge sharing within the RAM skill group, building capability and raising the bar on quality and consistency. Continuous Improvement: Contribute to process improvement, applying lessons learned to make future submissions faster, clearer and more impactful. Essential Skills/Experience Bachelor’s degree in science or a related field with 3+ years of regulatory experience within the biopharmaceutical industry or health authority General knowledge of drug development Strong project management skills Leadership skills, including experience leading multi-disciplinary project teams Excellent written and verbal communication skills Cultural a