Leads clinical operations for a key asset across its full lifecycle, setting the operational strategy and ensuring high-quality, on-time delivery of clinical studies. Works cross-functionally to align study execution with scientific and regulatory goals, driving innovation and efficiency while managing risk and stakeholder engagement. Focuses on patient-centric approaches and inspection readiness within a global, matrixed environment.
Leads clinical operations strategy and execution across the full lifecycle of a key asset, ensuring operational feasibility, regulatory compliance, and high-quality delivery of clinical studies. Works cross-functionally to align study design with scientific vision, manages vendor and resourcing strategies, and drives innovation in patient-centric trial execution. Serves as primary point of accountability for global clinical operations at the asset level.
Develop and maintain R packages and Shiny applications to support clinical trial data analysis and reporting workflows. Collaborate with statisticians and programmers to build reproducible, AI-enhanced tools, with a focus on open-source practices and modernization. Support user experience improvements and drive adoption through training and documentation.
Leads the development and execution of precision medicine strategies within global clinical programs, focusing on biomarker and diagnostic initiatives to support patient selection and regulatory submissions in neuroscience. Acts as a scientific expert, leading cross-functional teams and ensuring compliance with medical device regulations. Facilitates collaborations with external research partners and drives operational excellence in biomarker strategy implementation.
Lead clinical pharmacology and modelling & simulation efforts for infectious disease assets, applying pharmacokinetic and pharmacodynamic principles to support drug development from early stages through registration and lifecycle management. Develop population PK/PD and exposure-response models, guide dose selection, and present evidence to regulatory bodies. Work within cross-functional teams while maintaining hands-on involvement in quantitative analysis and strategic decision-making.
Lead and execute model-informed drug development strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize clinical trial design, dose selection, and regulatory submissions. Drive innovation in exposure-response analysis, population PK/PD, and quantitative systems pharmacology within a cross-functional R&D environment.
This role involves leading oncology clinical development for sarcoma, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety evaluation, contribute to regulatory interactions, and mentor clinical teams, ensuring patient-centred strategies within a global matrix environment. Deep expertise in sarcoma oncology and cross-functional collaboration are central to the position.
Lead clinical pharmacology and modelling & simulation efforts for infectious disease assets, applying pharmacokinetic/pharmacodynamic and exposure-response modelling to inform dose selection, trial design, and regulatory strategy. Work across development phases from early planning to lifecycle management, with a strong emphasis on hands-on quantitative analysis and scientific leadership within a cross-functional environment.
This role involves leading medical oversight in gastrointestinal (GI) oncology clinical development, ensuring patient safety and clinical integrity across study design, execution, and data interpretation. The Medical Director collaborates with cross-functional teams to integrate physician insights into clinical trials, engages with external experts and regulators, and contributes to regulatory submissions and scientific communications. The position requires deep expertise in oncology and clinical development within a global pharmaceutical environment.
This role involves serving as the physician lead within an oncology clinical development team, providing medical expertise in study design, safety oversight, and data interpretation for gastrointestinal (GI) cancer trials. The Medical Director ensures patient safety and clinical integrity across clinical studies, collaborates with cross-functional teams and external experts, and contributes to regulatory submissions and scientific communications. The position supports GSK’s mission to advance innovative cancer treatments grounded in disease biology and real-world impact.
Leads scientific and strategic integration across GSK's hematology oncology portfolio, ensuring cross-program alignment and innovation in clinical development. Provides expert guidance on disease biology, biomarker strategies, and trial design while shaping portfolio-level decision-making. Operates as a senior individual contributor interfacing with clinical teams, external experts, and regulatory bodies.
Leads cross-programme scientific strategy and integration across GSK’s hematology oncology portfolio, ensuring alignment in clinical development, biomarker strategies, and innovative trial design. Acts as a senior scientific partner to Clinical Development Leads and drives data-driven decision-making using emerging technologies like AI. Operates at the portfolio level to shape disease-area strategy and support regulatory and governance engagement.
Lead scientific and strategic integration across GSK's hematology oncology portfolio, ensuring alignment of clinical development programmes, biomarker strategies, and innovative trial designs. Drive cross-asset coordination and decision-making at the disease level, leveraging deep oncology expertise and emerging technologies like AI. Engage with internal stakeholders and external experts to shape portfolio direction and regulatory strategy.
This role leads cross-programme scientific strategy and integration across GSK’s hematology oncology portfolio, ensuring alignment in disease biology, biomarker development, and clinical trial innovation. The individual will drive portfolio-level decision-making, shape clinical development approaches using emerging technologies like AI, and engage with external experts and regulatory bodies. It is a senior individual contributor position focused on strategic coherence across multiple assets rather than direct management of a single programme.
The Variation Planning Process Manager will lead the design and implementation of Variation Planning processes within GSK’s ERP Evolution Programme, focusing on S/4HANA integration across Rx and Vx. The role involves defining end-to-end process frameworks, aligning with cross-functional teams including PLM, Quality, and Regulatory, and ensuring compliance with supply chain and regulatory requirements. Key responsibilities include process documentation, testing, change management, and transition planning from interim to future-state operations.
