The convergence of science and technology is changing discovery and development at GSK, allowing us to make advances on behalf of patients that were once thought impossible. Our R&D organisation is delivering more innovation, better and faster, using new data and platform technologies that speed discovery and development and improve the chance of success.

Reporting to the VP and Head of Clinical Pharmacology and Quantitative Medicine (CPQM) within the Respiratory, Immunology & Inflammation Research Unit (RIIRU), the VP, Digital Medicine is a critical leadership role responsible for defining and executing a compelling, future-focused digital strategy. The core purpose of this role is to spearhead the integration of digital tools—including wearables and remote monitoring—into clinical trials, enhancing study design, improving patient engagement, and navigating regulatory frameworks to maximize the likelihood of success.

Continuously evaluating emerging health technologies, including devices and applications to our key therapeutic areas of interest, as VP, Digital Medicine you will ensure GSK is always in a front running position.  You will forge ‘preferred partner’ relationships with external stakeholders including vendors, key opinion leaders, academic and clinical partners, to optimise GSK’s strategy and technology capabilities via access to the latest innovations as well as enhancing GSK’s reputation in this field.

Leading a multidisciplinary, global team accountable for end-to-end process digital strategy you will successfully collaborate with multiple matrix partners to ensure key transversal activities are executed to drive performance and delivery of the portfolio.  This is an exciting opportunity to bring your vision and leadership skills to profoundly impact patient outcomes through all that digital innovation has to offer.

This is an exciting opportunity to bring your vision and leadership to a new era of digital innovation in clinical pharmacology and quantitative medicine, profoundly impacting patient outcomes and shaping the future of R&D at GSK.

Key responsibilities

• Strategic Vision & Leadership
  Develop and communicate a clear, aspirational vision for digital health innovation within the CPQM organization, ensuring alignment with GSK’s mission to deliver transformative outcomes for patients.
• Digital Endpoint Development
  Conceive, validate, and implement novel digital endpoints across all phases of clinical development, from analytical and clinical validation studies to incorporation into late-phase trials, ensuring endpoints are clinically meaningful, regulatory-acceptable, and enhance patient experience.
• Clinical Pharmacology Integration
  Collaborate with clinical pharmacologists and quantitative scientists to embed digital health solutions into study design, enabling robust pharmacokinetic/pharmacodynamic (PK/PD) modeling, dose optimization, and the identification and validation of novel digital endpoints.
• Innovation & Capability Building
  Build and scale industry-leading digital health capabilities, including advanced analytics and AI/ML, to support high-volume, high-dimensional data analysis and real-time decision-making.
• Portfolio Impact & Operational Excellence
  Map digital clinical initiatives to high-priority pipeline areas, optimizing impact and value across R&D. Lead a multidisciplinary, global department to ensure end-to-end digital strategy execution and successful delivery of the portfolio. Influence throughout the enterprise matrix of GSK’s Translational Medicine, Clinical Science, Global Clinical Operations, Research Technologies, and digital and data teams such as AIML and Tech to elevate performance via successful execution.
• External Partnerships & Reputation Building
  Forge ‘preferred partner’ relationships with external stakeholders, including technology vendors, key opinion leaders, academic and clinical partners, to access the latest innovations and position GSK as a leader in digital medicine.
• Patient-Centric Design
  Incorporate the voice of the patient into digital clinical trial design, enhancing recruitment, retention, data quality, and the identification of unmet needs.
• Regulatory Strategy & Compliance
  Lead engagement with regulatory agencies to define evidentiary standards for digital endpoints and ensure compliance with evolving legal, ethical, and data protection frameworks.
• Resource & Risk Management
  Identify and align resources (people and financial), set team objectives, and manage risk to ensure successful project completion. Balance innovation with cost, risk, and compliance.
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