At a Glance
- Tasks: Lead the development of innovative digital products for evidence and regulatory content.
- Company: Join GSK, a global biopharma leader with a mission to impact 2.5 billion lives.
- Benefits: Flexible working culture, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment focused on innovation and patient impact.
- Why this job: Make a real difference in healthcare by driving AI-enabled product strategies.
- Qualifications: Master’s degree and extensive experience in digital product management required.
The predicted salary is between 90000 - 110000 £ per year.
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.
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
- 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.
Basic Qualifications
- 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 sizeable budgets and vendor portfolios.
- Proven people-leadership experience, including line-managing and building high-performing product teams.
- Experience delivering AI, data and analytics-enabled products on modern data platforms and cloud technologies.
- Experience operating in a GxP / validated-systems context, with strong data integrity, quality and compliance judgement.
Preferred Qualifications
- Deep experience with structured content management, modular document design or publications-management systems.
- Hands-on experience with AI-assisted authoring or NLP-based solutions, particularly in regulated or scientific content domains.
- Familiarity with GxP and validation expectations for systems used in regulatory submissions and evidence generation.
- Demonstrated executive influence with VP/SVP-level stakeholders to drive complex technology decisions and adoption.
- Experience scaling Agile ways of working across global, multi-disciplinary teams and managing strategic technology vendor partnerships.
Skills
- Agile Methodology
- Cross-Functional Teamwork
- Data Analysis
- Design Thinking
- DevOps
- Prioritization
- Product Development Research
- Product Roadmapping
- Project Management
- Return on Investment (ROI)
- Software Development
- Strategy Deployment
- User Experience (UX)
- User Interface (UI) Design
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 we're 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.
Product Director, Evidence Preparation in London employer: GlaxoSmithKline plc
GSK is an exceptional employer that fosters a culture of innovation and collaboration, making it an ideal place for professionals seeking to make a meaningful impact in the biopharma industry. With a commitment to employee growth through continuous learning opportunities and a flexible hybrid working model, GSK empowers its workforce to thrive while contributing to groundbreaking advancements in healthcare. Located in vibrant London, employees benefit from a dynamic work environment that prioritises ambition for patients and accountability for results.
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We think this is how you could land Product Director, Evidence Preparation in London
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We think you need these skills to ace Product Director, Evidence Preparation in London
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