Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

Site Name: USA - Pennsylvania - Upper Providence, Durham Blackwell Street, GSK HQ, Switzerland - Zug, UK – London – New Oxford Street, USA - Massachusetts - Waltham Posted Date: May 29 2026 For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain market positioning. Specifically, evidence must be generated and maintained throughout the product lifecycle as the standard of care changes, new competitors are introduced, and patents expire on existing competitors. The landscape is evolving quickly as trials demonstrating efficacy in an area of unmet need may receive expedited review, or orphan product status designation which affects both GSK and competitors launch timelines and approval requirements. More of our customers are developing sophisticated internal health outcomes capabilities and access to real world data that can be used to better understand unmet needs and real‑world effectiveness of our medicines. We need to better understand how our customers define value and to effectively collaborate with them to ensure we are generating value evidence data that includes real world evidence and cost‑effectiveness analyses that are impactful for payers, health systems, providers, and patients. The role of Director, Global Real‑World Evidence & Health Outcomes Research Scientist is critical to achieving this ambition by supporting asset teams to ensure that each medicine GSK brings to market is supported by scientifically credible, high quality evidence that drives competitiveness and strong evidence‑based product positioning, value propositions and value‑based pricing. The role is critical to support the alignment of evidence with evidentiary requirements of customers responsible for marketing authorization, recommendation and reimbursement leading to successful patient access, product use and commercial success. The role will report directly into the Senior Director, Global Real‑World Evidence & Health Outcomes Data Generation Lead for a complex priority asset and will have expertise in real‑world evidence and other non‑interventional study methods. The role will be a key member of the asset team and other relevant matrix leadership teams. The Director, Global Real‑World Evidence & Health Outcomes Scientist will be accountable for engaging closely with medical and matrix stakeholders and partner effectively in data generation plan (DGP) planning, design, execution, translation and dissemination at the study level for the asset. Responsibilities Plan, design and execute multiple studies for a given asset and manage timelines, deliverables, and budget. Assure quality of deliverables, including review and sign off project specifications, protocols, data analysis plans, final study reports, abstracts, posters and manuscripts, in adherence to SOPs. Identify resources, references and analyses to inform scientific design and advise internal experts (medical affairs, clinical, commercial/market access) and external experts as needed in support of the asset team. Translate needs for evidence into study concepts in alignment with strategic objectives and vision for the asset, e.g. development of study protocols and proposing innovative and cost‑effective ways of developing and executing studies. Develop and maintain a good working knowledge of real‑world data resources, existing partnerships and public initiatives and become the point person for select sources to advise on their suitability to address given research questions. Develop a deep understanding of customers’ needs, including clinicians and HTA requirements, and their acceptance of different types of evidence and impact of that evidence to their decision making. Collaborate with internal teams and participate in best practice sharing sessions across the non‑interventional study organization. Build strong working relationships with stakeholder groups across medical, market access, R&D and commercial to ensure strategic alignment and optimal cross‑functional collaboration and communication. Ensure key stakeholders, including TA aligned business leaders, are regularly updated on plans through periodic reporting. Develop excellent working relationships with external thought leaders to ensure appropriate methods and research agendas are applied, in accordance with GSK policies. Basic Qualifications MSc, or equivalent in health outcomes, health economics, epidemiology, pharmacy, health or life sciences. 5+ years of experience working in the pharmaceutical industry, preferably in a multi‑national company. Experience in planning and delivering individual projects, managing budgets and working within a matrix setting. A history of designing a variety of RWE studies including prospective observational studies, cross‑sectional and retrospective cohort studies, chart reviews, and database analyses. Proficiency in utilizing evidence for the development of global HTA submissions, reimbursement and/or medical engagements. A track record of delivering robust payer evidence and credibility to engage meaningfully with external experts and leaders in the field. Expertise with the diversity and complexity of healthcare markets, health technology assessment agencies, and reimbursement decision making globally, in region and local markets. Experience in communicating technical and complex concepts and results to various audiences to impact decision‑making. Experience in oncology. Preferred Qualifications Advanced scientific degree, e.g. PhD, PharmD or equivalent in Health Economics, Outcomes Research, Epidemiology or similar. Experience in Global and Country roles in oncology. What we value in you Clear, direct communication. You explain complex ideas simply and precisely. Collaborative mindset. You work well across functions and with external experts. Practical rigor. You balance scientific quality with timely, decision‑ready outputs. Inclusive leadership. You build trust, support colleagues’ development, and seek diverse perspectives. Curiosity and continuous learning about methods, data sources and payer needs. Salary and Benefits If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $204,000 to $340,000. If you are based in another US location, the annual base salary range is $204,000 to $340,000. 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 annual bonus and eligibility to participate in our share‑based long‑term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process. Equal Opportunity Employer 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. #J-18808-Ljbffr GSK