US Senior Medical Director - COPD Biologics

About this role

Senior Medical Director, COPD Biologics Introduction to the role Are you ready to provide senior medical leadership in an area with significant unmet patient need?

The Senior Medical Director, COPD Biologics will provide strategic medical leadership for AstraZeneca’s COPD biologics portfolio across the product lifecycle. As a senior member of US Medical Affairs and the US Core Medical Team , you will shape COPD biologics strategy, align medical priorities with patient needs and emerging science, and translate complex clinical insights into actionable plans.

Working closely with the US Medical Director, COPD Biologics , you will guide US medical plan development, launch readiness, evidence generation, external scientific engagement, and lifecycle management for current and pipeline biologics.

Accountabilities Strategic planning and asset leadership • Provide senior medical leadership for the US Brand Medical Plan across pre-approval, launch, and post-approval stages. • Shape US brand strategy, asset plans, launch readiness, lifecycle management, and Core Medical Team priorities. • Translate COPD biology, clinical data, and treatment landscape insights into clear US medical strategies.

Team leadership and capability building • Provide leadership, coaching, and mentorship to Medical Affairs colleagues, including the Medical Director, COPD Biologics. • Build team and Field Medical capability through scientific training, clinical education, and effective communication. • Promote accountability, innovation, inclusion, collaboration, and continuous improvement.

Pre-approval medical affairs • Provide senior US medical input into late-stage clinical development, endpoint relevance, subpopulation strategy, biomarkers, and launch readiness. • Support regulatory readiness through medical review, scientific positioning, data interpretation, and collaboration with Regulatory Affairs and global partners. • Develop compliant pre-approval scientific engagement strategies and partner on early value-evidence priorities for the US healthcare environment.

Post-approval medical affairs • Lead post-approval medical strategy, scientific exchange, Phase 4, real-world evidence, effectiveness, and lifecycle management priorities. • Guide publication strategy, congress planning, scientific response, data dissemination, medical education, and compliant material review. • Maintain the evolving US product scientific narrative using clinical data, guidelines, real-world insights, and emerging science.

External engagement and scientific leadership • Develop US external engagement strategy across experts, academic institutions, health systems, professional societies, and patient organizations. • Build credible peer-to-peer relationships and lead advisory boards and scientific exchange activities. • Serve as an appropriate US medical spokesperson while ensuring engagement is rigorous, balanced, patient-focused, and compliant.

Evidence generation and medical governance • Collaborate on clinical effectiveness studies, real-world evidence, health outcomes research, and externally sponsored research governance. • Provide medical input into product safety strategy and ensure Medical Affairs activities comply with US regulations, PhRMA Code, and AstraZeneca policies.

Enterprise and cross-functional leadership • Provide medical and scientific thought leadership across Medical Affairs, Clinical Development, Commercial, Regulatory, Market Access, HEOR, and related functions. • Influence strategic decisions through scientific reasoning, sound judgment, and understanding of the clinical, regulatory, and healthcare landscape. • Represent US medical needs with global teams and contribute to broader enterprise Medical Affairs priorities.

Minimum requirements • Medical, Pharmacy, or relevant scientific degree, such as MD, MBBS, PharmD, PhD, or equivalent education. • At least eight (8) years of relevant experience in Pulmonary Medicine, respiratory pharmacology, immune-mediated disease, clinical development, Medical Affairs, or a related pharmaceutical, biotechnology, or healthcare environment. • Significant experience leading Medical Affairs strategies and functions, including experience across late-stage clinical development, launch readiness, and/or post-approval Medical Affairs. • Demonstrated expertise in COPD, respiratory medicine, biologic therapies, or a closely related therapeutic area. • Strong understanding of the US regulatory and compliance environment, including FDA and OPDP requirements, the PhRMA Code, and applicable Medical Affairs standards. • Demonstrated ability to engage with and influence senior leadership and contribute to strategic business and medical decisions. • Proven ability to build trusted relationships with external experts, investigators, professional societies, academic institutions, patient organizations, and other healthcare stakeholders. • Experience leading through cross-functional and matrixed ways of working, with the ability to align diverse stakeholders around shared scientific and patient-focused priorities. • Demonstrated ability to develop talent, provide mentorship, inspire followership, and drive accountability. • Lead and influence perceptions constructively, solve complex problems, and implement innovative Medical Affairs approaches that improve patient care and outcomes. • Lead medical, scientific, clinical, and technical evaluation data insights. • Extensive experience in interpreting medical and scientific literature and designing effective medical and communication strategies accurately and clearly. • Understanding of early- and late-stage clinical development, evidence generation, and product lifecycle management. • Ability to work effectively in a multicultural, international, and agile organization. • Willingness to travel approximately 20–25% on average within the US and occasionally internationally.

Preferred requirements • Board certification or eligibility in Pulmona

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