GSK Development and Chief Medical Officer (CMO) Digital and Technology’s mission is to disrupt and transform the way GSK thinks about, generates and submits evidence to radically accelerate the delivery of medicines and vaccines for our patients and participants. We act as a strategic thought partner for the Development and CMO organizations, bringing together diverse stakeholders to radically transform and connect siloed processes using innovative and integrated technology. Our Senior Product Director, Evidence presentation and submission will act as technology disruption thought leaders, accountable for partnering with business stakeholders to reimagine end-to-end ways of working using technology. They are accountable for curating, championing, and managing 3-year product vision for a dynamic portfolio of technology products and owning these products across the entire lifecycle, working in partnership with internal and external technology delivery partners. As the Senior Product Director for Evidence Presentation & Regulatory, you will own the product strategy for the final, critical mile of our clinical pipeline. This portfolio provides the technology that transforms our scientific evidence into high-quality regulatory submissions and manages our dialogue with health authorities and the public worldwide. You will be accountable for setting the vision and roadmap across two core capabilities: Medical and Regulatory Content Lifecycle: Driving the end-to-end lifecycle of our submission content. This includes the platforms that enable AI-assisted content generation, collaborative authoring, and robust text-based content management, as well as the systems for formatting, quality control, and securely transmitting electronic submissions to global health authorities. Regulatory Engagement & Intelligence: Empowering our regulatory teams with the intelligence and tools needed to effectively engage with global health authorities and improve GSK pipeline success. This encompasses the systems that manage regulatory intelligence, tools to manage the lifecycle of health authority questions, and the platforms that ensure compliance with our public transparency and data disclosure commitments. Your mandate is to drive a cohesive strategy that innovates with AI and automation to accelerate the submission lifecycle, enhance the quality and consistency of our regulatory filings, and create a world-class intelligence platform to inform our regulatory strategies.
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Job Type
Full-time
Career Level
Director
Number of Employees
5,001-10,000 employees