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
Task Execution Under Pressure, Makes strategic Business Decisions, Business accumen, Commercial Awareness, Objective Setting, Accountability, Consumer Insight, Creative Direction, R&D, Change Leadership, Product Lifecycle Management, Intellectual Property, Business Partnership, Collaboration and partnership building, Relationship Management, Adapt to changes in technological development plans, Ability to challenge the status quo and propose improvement, Innovation Processes, Digital transformation for R&D, Quality and Manufacturing.
What we offer
With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way.
We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.
Equality
We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you.
All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.
Job Segment
Public Health, Epidemiology, Clinical Research, Medical Research, Counseling, Healthcare
Apply now »
Apply now
Start apply with LinkedIn
Apply Now
Start
Please wait...
Find similar jobs
R&D_gb
Legal Terms & Conditions
Privacy Notice
About Us
Fraud Notice
Opens in a new tab.
Opens in a new tab.
Opens in a new tab.
Opens in a new tab.
Opens in a new tab.
© Reckitt Benckiser Group plc | Registered office at 103 - 105 Bath Road, Slough, Berkshire, SL1 3UH | Registered in England & Wales, No 6270876