Description
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 and publications.
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.
Responsibilities:
- Own the product vision and roadmap for content generation and collaboration
- Bring deep domain expertise across the evidence and regulatory content lifecycle
- Drive structured content capabilities
- Shape scalable architecture with architects and engineers
- Champion an AI-first approach
- Own delivery end-to-end
- Embed quality, risk and compliance
- Build trusted partnerships and influence at VP/SVP level
Basic Qualifications:
- Master’s degree or equivalent experience in a scientific, technical or quantitative discipline
- ~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
- Proven people-leadership experience
- Experience delivering AI, data and analytics-enabled products
- Experience operating in a GxP / validated-systems context
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
- Familiarity with GxP and validation expectations for systems used in regulatory submissions and evidence generation
- Demonstrated executive influence with VP/SVP-level stakeholders
- Experience scaling Agile ways of working across global, multi-disciplinary teams