Product Director, Evidence Preparation

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About the role

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. We’re uniting science, technology, and talent to get ahead of disease together. Find out more: Our approach to R&D Position Summary As Product Director, you are accountable for the digital products that enable structured, collaborative and increasingly automated authoring of evidence and regulatory content — across clinical, non-clinical, CMC, safety, regulatory (including labelling) and publications. Sitting within R&D Digital & Technology, you translate the needs of Medical Writing, Regulatory, Safety, CMC, Clinical and Publications stakeholders into a coherent, AI-enabled product vision. You set the strategy and roadmap, lead and develop your product portfolio, and act as technical SME for the programmes that deliver these capabilities. You influence at VP/SVP level and role-model GSK’s values — Ambitious for patients, Accountable for impact, Do the right thing . Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: • Own the product vision and roadmap for content generation and collaboration, aligned to the Evidence Presentation & Regulatory strategy and translated into clear value hypotheses, OKRs and prioritised backlogs. • Bring deep domain expertise across the evidence and regulatory content lifecycle — clinical, non-clinical, CMC, safety, regulatory (including labelling) and publications — using that insight to make sharper product decisions. • Drive structured content capabilities — tackling bottlenecks and opportunities in structured content management, modular authoring and component reuse that improve the quality, consistency and speed of evidence preparation. • Shape scalable architecture with architects and engineers on technical trade-offs, designing scalable, reusable services and bringing emerging technology into the portfolio where it creates value. • Champion an AI-first approach — making AI, NLP and analytics default tools for AI-assisted authoring, automation and decision support, with robust validation of AI outputs and a sound grasp of the submission data landscape. • Own delivery end-to-end — sequencing the backlog and release plan to validate authoring hypotheses and scale proven features across asset teams; contracting vendors on outcomes and holding teams to account for quality, pace and measurable value. • Embed quality, risk and compliance — GxP, privacy and AI governance — from the outset, ensuring transparent, auditable platforms and good hygiene in core systems of record. • Build trusted partnerships and influence at VP/SVP level across Medical Writing, Regulatory, Safety, CMC, Clinical and Publications; coach and grow a high-performing, multi-disciplinary team, role-modelling GSK’s values and an inclusive, psychologically safe culture. Why You? Basic Qualifications We are seeking professionals with the following required skills and qualifications to help us achieve our goals: • Master’s degree or equivalent experience in a scientific, technical or quantitative discipline (e.g. life sciences, computer science, engineering, mathematics). • ~10+ years leading technology-focused transformation and ~5+ years of progressive experience in digital product management and leadership. • Significant life-sciences experience with direct exposure to regulatory, clinical development or related functions. • Track record of owning and scaling enterprise digital products, operating with

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