Statistician
Reckitt BenckiserJob Description
Statistician
We are Reckitt
Research & Development
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
About the role
We are seeking a highly analytical and scientifically driven Statistician to join our Evidence Generation & Clinical Research team. In this role, you will provide expert statistical leadership across clinical and research programs, supporting the generation of robust evidence that informs product development, substantiates product claims, and supports regulatory requirements.
Working closely with cross-functional stakeholders including Medical Affairs, Clinical Research, Regulatory Affairs, and external research partners, you will be responsible for designing and executing statistical analyses, developing study methodologies, and ensuring the delivery of high-quality scientific evidence. You will play a critical role in translating complex data into meaningful insights that drive business and consumer health outcomes.
Your responsibilities
- Provide expert statistical support across clinical research, evidence-generation, and innovation projects.
- Design, develop, and review study protocols, Statistical Analysis Plans (SAPs), topline reports, and Clinical Study Reports (CSRs).
- Perform and interpret statistical analyses using primary and secondary healthcare, consumer, and clinical data.
- Apply appropriate statistical methodologies, models, and analytical techniques to generate robust scientific evidence and support product claims.
- Collaborate with cross-functional teams including Medical Affairs, Clinical Operations, Regulatory Affairs, and R&D to ensure alignment on study objectives, endpoints, and evidence strategies.
- Support the design, validation, and implementation of Clinical Outcome Assessments (COAs), Patient-Reported Outcomes (PROs), and other clinical measures.
- Generate evidence to support product registration, claims substantiation, and business decision-making.
- Manage and oversee statistical deliverables from external vendors, CROs, and research partners, ensuring quality, timelines, and budget adherence.
- Ensure compliance with regulatory guidelines, quality standards, and internal SOPs.
- Contribute to the development and continuous improvement of statistical processes, methodologies, and best practices.
- Communicate complex statistical concepts and study results effectively to technical and non-technical stakeholders.
- Support the Statistics Manager in delivering portfolio objectives and advancing evidence-generation capabilities across the organization.
The experience we're looking for
- Bachelor's degree in Statistics, Biostatistics, Mathematics, Epidemiology, Data Science, or another quantitative discipline.
- Master's degree in Statistics, Biostatistics, or a related field preferred.
- 5+ years of experience in biostatistics, medical statistics, clinical research, pharmaceuticals, consumer healthcare, or life sciences.
- Hands-on experience supporting clinical trials, observational studies, real-world evidence studies, or evidence-generation programs.
- Strong understanding of clinical trial design, statistical methodologies, hypothesis testing, and study reporting.
- Experience developing and reviewing Protocols, SAPs, CSRs, and statistical outputs.
- Proficiency in statistical software such as SAS, R, Python, or equivalent analytical tools.
- Knowledge of regulatory and industry guidelines related to clinical research and evidence generation.
The skills for success
What we offer
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