Drives an AI-native strategy for clinical development operations, defining where AI adds value, building working prototypes hands-on, and moving priority capabilities into production. Combines strategy, agentic AI engineering (Python, SQL, LLM APIs, Azure/AWS) and vendor build-buy-partner decisions, reporting to the Head of Asset Acceleration and AI.
Drives an AI-native strategy for clinical operations, defining where AI adds value, building working prototypes hands-on, and taking priority capabilities into production. Combines strategy, agentic AI engineering (Python, SQL, LLM APIs, MCP, Azure/AWS) and vendor build-buy-partner decisions, working with business SMEs, enterprise technology teams and R&D leaders.
Develops, validates and runs ligand-binding and cell-based bioanalytical assays generating pharmacodynamic and immunogenicity data for clinical mRNA programmes. Works in a GcLP-regulated lab using Thermo Watson LIMS and electronic notebooks, handling clinical samples, critical reagents, SOPs and validation reports while partnering with Clinical Operations and Sample Management.
Owns defined planning process areas within GSK's ERP Evolution Programme, ensuring the global S/4 Planning template integrates with OMP, APO and other planning tools across Rx and Vx supply chains. Leads design, configuration input, documentation, testing, data migration and business readiness for UAT, cutover and post-go-live support, working with SAP functional experts, GPO, PLM, Quality and site teams.
Accountable for GSK R&D's enterprise portfolio of external scientific content and data licenses, managing budget, forecasting, cost controls and vendor commercial terms. Acts as senior interface to information providers and connector across scientific, procurement, legal, copyright and technology teams, keeping published-information use copyright-compliant. Positions the portfolio for AI and text-mining exploitation, anticipating future licensing needs.
Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Designs, oversees and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, analysis plans and interpretation. Manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.
Lead epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Design, oversee and deliver observational and database studies using real-world data, registries and linked sources, while managing external vendors, budgets and timelines and preparing regulatory documents and publications.
Owns integrated Regulatory Development Plans in Planisware for GSK's HIV medicines portfolio, translating regulatory strategy into executable timelines, dependencies and deliverables. Manages FTE/resource and external project expenditure forecasting, scenario planning and portfolio insights to support governance cycles and decision-making. Partners with Global Regulatory Leads, Clinical, Safety, CMC and Finance stakeholders in a complex matrix environment.
Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with cross-functional partners. Designs, oversees and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, data needs and analysis plans. Manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.
Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Designs and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, analysis plans and interpretation. Manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.
Develops and executes global and regional regulatory strategies for oncology assets, ensuring optimal labelling and approvals while maintaining compliance. Partners with the Global Regulatory Lead and cross-functional teams to shape development plans and regulatory interactions across multiple regions, assessing regulatory intelligence and competitive landscape to inform decisions.
Develops and executes global and regional regulatory strategies for oncology assets, ensuring optimal labelling, approvals and lifecycle compliance. Partners with the Global Regulatory Lead, therapeutic area head and cross-functional teams to shape development plans and regulatory authority interactions across multiple regions, while driving process improvement and innovation.
Develops and executes global and regional regulatory strategies for oncology assets, ensuring optimal labelling, approvals and lifecycle compliance. Partners with the Global Regulatory Lead and cross-functional teams on submissions, health-authority interactions and regulatory intelligence across multiple regions. Hybrid role based in London, Stevenage, Baar or Wavre.
Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Designs, oversees and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, data needs and analysis plans. Also manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.
Manages statistical planning and delivery across oncology clinical programs, designing trials and analyses that shape development decisions and regulatory strategy. Works with clinical, regulatory, safety and clinical pharmacology teams, using simulation and advanced methods in R or Python, and mentors statisticians. Based in London or Stevenage, with a planned relocation to Cambridge by early 2029.
