Senior Product Owner – Content Generation & Collaboration

Overview

In this role you will lead digital products that enable structured, collaborative and increasingly automated authoring of scientific and regulatory content across clinical, CMC, safety, regulatory and publications. You translate user needs into a prioritised backlog, shape an outcome-focused roadmap and own the value case for your products. You will be a technology partner within a major programme, mentor other Product Owners and model GSK’s values. You will drive AI-enabled discovery and authoring while ensuring quality, compliance and data integrity.

Responsibilities

• Co-create the product vision and roadmap for content generation and collaboration with business stakeholders, owning objectives, key results and the value case
• Apply domain understanding of the evidence and regulatory content lifecycle to define problems and user needs
• Develop structured content capabilities (modular authoring, component reuse) to improve speed and consistency of evidence preparation
• Partner with architects and engineers on technical decisions and manage dependencies and risks
• Apply AI-first approaches to accelerate backlog decisions, coaching on responsible prompting and value justification
• Own end-to-end delivery (milestones, budget, roadmap, quality) and validate value via pilots before scaling
• Embed quality, data integrity, privacy, GxP and AI governance in delivery and assess risks before releases
• Collaborate across Medical Writing, Regulatory, Safety, CMC, Clinical and Publications; mentor junior Product Owners and foster an inclusive environment
• Manage strategic suppliers and partners to meet roadmap commitments and maintain GSK standards

Key requirements

• Bachelor’s degree or equivalent experience in a scientific, technical or related discipline
• Significant experience in digital product management or product ownership with ability to independently own vision and roadmap
• Hands-on product management with backlog ownership and writing clear user stories and acceptance criteria
• Experience in pharmaceutical R&D, clinical development or regulatory affairs with exposure to scientific or regulatory content authoring
• Proven track record of end-to-end delivery for digital products including pilots or value proofs
• Strong understanding of enterprise app architecture, integrations/APIs, cloud environments, data flows and non-functional requirements
• Working knowledge of GxP/validated systems with data integrity judgement
• Experience partnering with architects/engineers on technical trade-offs and sense-checking estimates
• Demonstrated ability to work in global, matrixed organisations and influence cross-functional teams

• Cross-functional collaboration
• Storytelling with data
• Mentoring and coaching
• Structured content and component management
• Modular document design
• Publications-management systems (e.g. Veeva Vault, Certara CoAuthor, Arbortext)

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