Description
Job descriptionSite Name: USA - Pennsylvania - Philadelphia, Belgium-Wavre, UK - London, USA - Massachusetts - Waltham, USA - North Carolina - Durham
Posted Date: Oct 30 2025
The Principal Statistician RWB is a global role responsible for driving strategic initiatives for value delivery. This role applies advance biostatistical methods and AI tools to real world data (RWD), to generate real world evidence (RWE) for informing trial design, regulatory submissions, reimbursement and safety signals.
The strategic role works in close partnership with cross-functional teams across the GSK and is tasked with leading the development and optimization of RWE strategies for priority assets. The role is pivotal in ensuring data-driven decision-making generates the best evidence package for approvals.
Key Responsibilities:
Biostatistics:
As a Project Biostatistician, lead the design and analysis of non-interventional studies, aligning with cross functional teams, managing timelines, and ensuring methodological rigor and quality control.
Apply statistical and RWD expertise to guide the selection and appropriate use of complex health data sets, co-develop variable definitions, code lists, and author technical specification documents.
Develop and refine statistical analysis plans, conduct complex statistical analyses, including for example causal inference, comparative effectiveness, target trial emulation, and communicate findings to internal and external stakeholders.
Strategic Initiatives:
Serve as a RWB consultant within matrix teams, leveraging in-depth expertise on assigned assets.
Serve on enterprise level strategic initiatives, for example Disease Area Acceleration Teams, for organizational deliverables.
Communication:
Present statistical analyses and insights effectively to internal stakeholders and external audiences, including conferences and publications, showcasing the value of biostatistical contributions.
Engage in strategic communication to reinforce the role of biostatistics in driving innovation and decision-making across the organization.
Methodological Development and Innovation:
Stay informed on emerging industry trends and incorporate cutting-edge biostatistical methods to improve study designs and analytics.
Conduct methodological research and contribute to the development/application of new analytical techniques.
Regulatory Support and Compliance:
Provide biostatistical expertise on RWD during regulatory submissions, preparing for meetings and addressing regulatory queries to ensure compliance with industry standards.
Stay current with regulatory guidance on the use of RWD for decision-making and advise on statistical approaches aligned with regulatory expectations.
Why You?
Basic Qualifications:
PhD or Master's degree in Statistics, Data Science, Epidemiology, or related field.
PhD with 3+ years work experience / Master's degree with 5+ years in the pharmaceutical/biotech industry, preferably in real-world evidence, epidemiology, or health outcomes research.
Experience working with drug development processes utilizing statistical skills to achieve project and business objectives.
Experience using RWD (e.g., electronic health records, insurance claims, registries) and applying observational study designs and biostatistical principles in clinical/epidemiological research.
Experience in programming languages R and SQL, working with observational datasets.
Experience contributing to methodological research and publications in the field of biostatistics and real-world data analytics.
Preferred Qualifications:
Experience working within regulatory frameworks related to RWD.
Experience in advanced biostatistical techniques, including causal inference, comparative effectiveness, time to event analysis, longitudinal and predictive modelling, and external control arms.
Familiarity with machine learning techniques and applications in real-world data analysis.
Demonstrated ability to manage complex projects and deliver high-quality results in dynamic environments.
Strong communication and interpersonal skills to effectively convey complex statistical concepts.
Fluency in written and spoken English.
Why Join Us?
At GSK, we are united by a shared purpose: helping people do more, feel better, and live longer. As Associate Director/Principal Statistician of Real-World Biostatistics, you will play a key role in advancing pharmaceutical science and contributing to the development of life-changing medicines. GSK offers opportunities to work on cutting-edge projects, collaborate with talented teams, and drive innovation in healthcare.
Join us and make an impact. Apply today!
#LI-GSK
The US annual base salary for new hires in this position ranges from $119,625 to $199,375 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.Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
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