Sr Director, GMASE Portfolio Execution- Oncology

Job description

Business Introduction 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. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together. Find out more: Our approach to R&D Position Summary The purpose of the Global Monitoring & Site Engagement – Sr Director of Portfolio Execution – (Oncology) is to serve as the single accountable leader for therapeutic area execution within GMASE, translating R&D and therapeutic strategy into predictable, high-quality clinical delivery at scale. Operating within the DevOps model, this role owns GMASE’s execution outcomes for the therapeutic area, ensuring that clinical delivery moves from fragmented, study-by-study execution to a consistent, data-driven, and continuously connected delivery system across programs, countries, and partners. The position is accountable for how GMASE plans, deploys, and optimizes resources, site engagement, monitoring approaches, and risk management to deliver the therapeutic area portfolio, not for setting GSK therapeutic strategy or scientific direction. In close partnership with Disease Area Leaders (DALs), therapeutic area leadership, and DevOps counterparts, the position serves as GMASE’s execution lead, converting strategic intent into measurable improvements across GMASE’s value drivers — velocity, quality, predictability, expertise, and productivity. Through leadership of Global Program Leads and close coordination with Planning & Strategic Feasibility, GCSD, DS&M, Clinical Science, Regulatory, and external CRO partners, this position puts the DevOps operating model into practice within GMASE, positioning GMASE as the engine of continuous, AI-enabled evidence generation for the therapeutic area. Key Responsibilities Own therapeutic area execution for GMASE as a continuous, AI-enabled evidence generation engine, with full accountability for how the TA portfolio is delivered across programs, studies, countries, and partners in alignment with DevOps principles. Provide GMASE’s execution and delivery-feasibility input into Disease Area Strategy Plans, acting as GMASE’s senior execution counterpart to Disease Area Leaders (DALs) and TA stakeholders, representing GMASE in TA-level execution discussions, trade-offs, and delivery commitments, while partnering closely on priorities and outcomes. Establish GMASE TA-level execution alignment with Planning & Strategic Feasibility, ensuring portfolio priorities, commercial positioning, feasibility insights, and delivery strategies are coherently translated into executable, scalable plans. Own GMASE TA-level portfolio performance oversight, including setting expectations, reviewing execution signals and evidence assurance data, identifying systemic risks and constraints, and driving timely resolution through structured escalation and cross-functional decision-making. Provide senior leadership and talent stewardship for Global Program Leads (GPLs), including setting execution standards, strengthening decision quality, building leadership capability through fit-for-purpose onboarding and development, and holding accountability for performance; may include direct line management of GPLs. Ensure appropriate site engagement for the TA, building GMASE’s site network as durable infrastructure rather than a study-by-study relationship — defining with key stakeholders and overseeing GMASE TA-wide site engagement and relationship strategies, including site tiering aligned to enterprise priorities, focusing GMASE focuses effort where it most impacts velocity, quality, and predictability. Own GMASE’s execution governance for outsourced delivery within the TA, setting expectations with CRO partners, overseeing performance, and resolving delivery issues and escalations to ensure consistent, high-quality outcomes. Ensure GMASE effective cross-functional execution governance, connecting GPLs and study teams to the appropriate decision-makers across GCSD, DS&M, Clinical Science, Regulatory, and other partners to remove systemic barriers and prevent fragmented delivery. As a member of the GMASE Leadership Team, chair GMASE therapeutic area portfolio governance forums, including monthly TA reviews with Country Heads and functional partners, to drive performance transparency, resource alignment, and execution readiness, and contribute TA-level insight and recommendations to the Leadership Team. Maximize the use of AI-enabled tools and workflows across GMASE TA execution and monitoring to accelerate trial timelines, reduce trial costs, and reduce time spent on manual tasks, continuously optimizing resource deployment and monitoring approaches based on actual utilization and delivery needs. Why You? Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals Bachelor’s degree in life sciences, healthcare, business or a related field, or equivalent experience. Minimum of 10 years of pharmaceutical R&D or related industry experience. Extensive (8+ years) leadership experience in clinical operations within the relevant therapeutic area. Deep therapeutic area expertise and understanding of Respiratory/Immunology strategy, data, operational needs, and commercial positioning to enable aligned execution. Experience owning end-to-end execution outcomes at portfolio or TA level, including accountability for delivery tradeoffs, risk resolution, and performance. Preferred Qualification If you have the following characteristics, it would be a plus Advanced degree (Master’s, PhD, PharmD, MD) in a relevant discipline. Experience with real-world evidence, health economics and outcomes research, or epidemiology. Demonstrated ability to lead cross-functional teams, resolve complex issues, and drive study and portfolio performance. Strong global stakeholder management experience across GCSD, DS&M, Clinical Science, Regulatory, and country organizations. Proven experience coaching and developing operational leaders. Day-to-day fluency in using AI to accelerate trial timelines, improve data quality, evidence assurance, and reduce time spent on manual tasks. Risk Based Quality Management knowledge. Experience leading global portfolios or cross-region evidence programs. Strong data fluency, including experience using dashboards and performance metrics to drive decisions. Experience with vendor oversight and partnerships with CROs, academic networks or external investigators. Demonstrated success delivering process improvements or digital-enabled transformation in evidence generation. How to apply If this role matches your experience and ambitions, please apply. We welcome candidates from all backgrounds and experiences who share our mission to get ahead of disease together. We encourage you to tell us how your skills and experience will help deliver impact in this role. Skills Agile Thinking, Business Acumen, Clinical Development, Clinical Trial Designs, Communication, Creativity, Decision Making, Fostering Collaboration, Good Clinical Practice (GCP), Influencing Without Authority, People Management, Pharmaceutical Industry, Project Management, Study Design The US annual base salary for new hires in this position ranges from $189,750 to $316,250. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an a