Senior Product Owner – Content Generation & Collaboration

Team Introduction

You will join R&D Digital & Technology working at the intersection of Medical Writing Regulatory Safety CMC Clinical and Publications. This team designs and delivers digital products that transform how scientific and regulatory content is authored reviewed and submitted helping our R&D organisation work more efficiently compliantly and collaboratively.

Position Summary

As Senior Product Owner for Content Generation & Collaboration you will lead 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. You will translate complex user needs into clear requirements and a prioritised backlog co-create an outcome-focused roadmap and own the value case behind your products. You will represent technology for the content generation and collaboration workstream in a major strategic programme lead end-to-end delivery of your roadmap mentor other Product Owners and role-model GSKs values.

Key Responsibilities

• Co-create the product vision and roadmap for content generation and collaboration with business stakeholders owning objectives key results and the value case and continuously testing ideas before committing capacity.
• Bring strong domain understanding of the evidence and regulatory content lifecycle framing problems through jobs-to-be-done and challenging requirements that do not map to real user needs.
• Drive structured content capabilities including modular authoring component management and reuse to improve the speed quality and consistency of evidence preparation and authoring journeys.
• Lead as a technology partner shaping trade-offs with architects and engineers owning key technical decisions and managing technical dependencies non-functional requirements and technology risks alongside functional delivery.
• Work AI-first by using AI to accelerate discovery drafting and scenario analysis for backlog decisions coaching the team on responsible prompting and judging where AI-assisted authoring truly adds value versus risk.
• Own end-to-end delivery of your product including milestones budget roadmap and quality validating value early through proofs of value and pilots before scaling and ensuring technical readiness across development test/validation and production.
• Build quality and compliance into delivery safeguarding data integrity (ALCOA) embedding GxP privacy and AI-governance requirements throughout change and running risk assessments before major releases.
• Partner influence and mentor across Medical Writing Regulatory Safety CMC Clinical and Publications negotiating scope constructively using storytelling and data to land difficult messages and coaching junior Product Owners in an inclusive psychologically safe environment.
• Manage strategic technology suppliers and delivery partners to ensure deliverables technical quality documentation knowledge transfer and commitments support the roadmap and GSK standards.

Basic Qualifications

• Bachelors degree or equivalent experience in a scientific technical or related discipline (e.g. life sciences computer science engineering).
• Significant experience in digital product management or product ownership in progressively senior roles with the ability to independently own the vision roadmap and prioritisation for a complex workstream.
• Hands-on product management and backlog ownership including writing clear testable user stories and acceptance criteria running refinement with engineering and prioritising a backlog using structured methods (e.g. RICE WSJF MoSCoW).
• Experience in pharmaceutical R&D clinical development or regulatory affairs with direct exposure to scientific regulatory or medical content authoring.
• Proven track record of owning end-to-end delivery for digital products including value validation through pilots or proofs of value before scale-up.
• Strong understanding of enterprise application architecture integrations/APIs MCP cloud environments identity and access data flows and non-functional requirements enabling informed product decisions with engineering and architecture teams.
• Working knowledge of GxP / validated systems with sound data-integrity quality and compliance judgement.
• Experience partnering with architects and engineers on technical trade-offs with sufficient technical fluency to own product-level decisions and sense-check estimates.
• Demonstrated ability to work in global matrixed organisations and influence cross-functional teams.

Preferred Qualifications

• Hands-on experience with structured content and component management modular document design component reuse or publications-management systems (e.g. Veeva Vault Certara CoAuthor Arbortext).
• Experience with AI-assisted authoring or NLP-based solutions in regulated or scientific content domains.
• Familiarity with AI / ML solutions in regulated environments and associated validation and governance requirements.
• Experience leading a technology workstream within a large transformation programme in a complex enterprise environment.
• Familiarity with eCTD structured content standards or the wider submission data landscape (e.g. IDMP).

Closing date for applications: 5th November 2026

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Skills

Why GSK

Uniting science technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade as a successful growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.

People and patients around the world count on the medicines and vaccines we make so were committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients accountable for impact and doing the right thing is the foundation for how together we deliver for patients shareholders and our people.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race color religion sex (including pregnancy gender identity and sexual orientation) parental status national origin age disability genetic information (including family medical history) military service or any basis prohibited under federal state or local law.

We believe in an agile working culture for all our roles. If flexibility is important to you we encourage you to explore with our hiring team what the opportunities are.

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