Lead clinical pharmacology, modeling, and simulation efforts for infectious disease assets, driving dose selection and development strategy through population PK/PD and exposure-response modeling. Serve as a scientific leader within cross-functional teams while remaining hands-on with quantitative analyses. Contribute to regulatory submissions and advance model-informed drug development across the R&D lifecycle.
Lead clinical pharmacology and modelling & simulation efforts for infectious disease assets, applying quantitative methods to inform dose selection, trial design, and regulatory strategy. Work across development phases from early planning to lifecycle management, using population PK/PD and exposure-response modelling. Operate as a scientific leader within a cross-functional environment while remaining hands-on with data analysis and model development.
Design and develop microfluidic systems for a point-of-care diagnostic device that enables metagenomic sequencing through a cartridge-based interface. Work closely with cross-functional teams to integrate microfluidics with instrumentation, electronics, and firmware, focusing on robustness, automation compatibility, and real-world performance. Conduct prototyping, testing, and validation using techniques like soft lithography and rapid prototyping to advance decentralized infectious disease diagnostics.
Conduct independent, high-impact research in a multidisciplinary environment focused on engineering biology, with responsibilities including experimental design, data analysis, publication, and mentoring junior researchers. Work at the intersection of biology, technology, and engineering within a newly established, well-resourced institute pursuing transformative solutions in health, agriculture, and sustainability.
Lead statistical strategy for clinical development projects in inflammation and immunology, providing expert input on study design, analysis plans, and regulatory submissions. Collaborate with cross-functional teams to ensure robust data interpretation and compliance with global standards. Drive innovation in statistical methodology and support publication activities and product defense.
Leads statistical strategy and oversight for global clinical development projects in inflammation, immunology, and specialty care. Provides expert input on study design, analysis plans, and regulatory submissions while guiding cross-functional teams and external collaborators. Focuses on innovation in statistical methodology and ensures compliance with regulatory standards and internal processes.
This role involves working in a sterile production environment, either in aseptic or manufacturing operations. Responsibilities include operating advanced manufacturing systems, performing analytical tests, and maintaining aseptic conditions in cleanroom environments. Collaboration with cross-functional teams and continuous improvement are key aspects.
This role involves shaping and leading the adoption of AI and technology in GSK's R&D, connecting strategic initiatives with practical implementation. Responsibilities include building a small internal adoption team, establishing a hub-and-spoke model for cross-R&D initiatives, and ensuring measurable value from new technologies.
This role involves shaping and leading the adoption of AI and technology in GSK's R&D, connecting strategic initiatives with practical implementation. Responsibilities include building a small internal adoption capability, establishing a hub-and-spoke model for cross-R&D initiatives, and ensuring measurable value from new technologies.
This role involves partnering with leaders of priority technology programmes in R&D to clarify strategy, scope, and value objectives. You will provide an independent, evidence-based view of programme progress, risks, and value delivery, while helping teams solve strategic problems and remove barriers. The role requires significant experience in strategic technology, AI, and digital transformation in a pharmaceutical environment.
This role involves setting and governing end-to-end product quality strategy for business-critical assets, ensuring alignment across multiple functions and stakeholders. Responsibilities include leading product quality teams, representing quality in governance forums, and managing product quality risk throughout the lifecycle from development to commercialization.
This role involves leading the development and integration of end-to-end product quality strategies for critical pharmaceutical assets, ensuring alignment across multiple functions and stakeholders. Responsibilities include risk management, regulatory compliance, and strategic input for product launch and lifecycle activities.
This role leads the strategic transformation of CMC regulatory submissions at GSK, shaping the future of dossier development through innovation in automation, Generative AI, and structured data. The Senior Director will drive alignment across regulatory, quality, manufacturing, and technology functions, championing initiatives like ICH M4Q and Project Sonata. It involves influencing senior governance, leading change, and building next-generation regulatory processes in a global, science-driven environment.
Leads the strategic transformation of CMC regulatory submissions at GSK, driving innovation through automation, Generative AI, and structured data. Works cross-functionally to align regulatory strategy with development and enterprise initiatives, including ICH M4Q and Project Sonata. Focuses on modernising the 'CMC dossier of tomorrow' within a global matrix environment.
This role leads the strategic transformation of CMC regulatory submissions at GSK, shaping the future of dossier content and processes through initiatives like ICH M4Q and Project Sonata. The individual will drive innovation using automation, structured data, and Generative AI while aligning regulatory, development, and quality functions. It involves high-level stakeholder engagement and governance input across a global matrix organization.
