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Statistician (Part-time permanent)
Slough, Berkshire 
Competitive Salary & excellent benefits package 


This role will provide expert statistical input across the portfolio of work for EG&CR including but not limited to evidence brief, protocol, SAP, topline and CSR using consumer insights to meet business needs. Selecting and working efficiently and effectively with outsourcing partners ensuring high quality deliver on time to agreed costs, as well as providing data generation leadership across the business as required.




  • Part of the MAEG team and reports to Head of Statistics and Data Management, this role will be intrinsically involved in deciding how the consumer and business needs are met by using Clinical Trials or other approaches to generate knowledge and insights for stakeholders to be able to make decisions.
  • Provides technical expertise across Hygiene and Health category products and initiatives globally through an understanding of clinical, regulatory, and outsourcing requirements working alongside Clinical Operations colleagues.

The role is responsible for individual excellence in a team setting to design and deliver the innovation portfolio as well as develop sounds statistical thinking in the wider Reckitt medical team and beyond.


Insight & Evidence 

  • Provide expert statistical input to the project evidence plan ensuring scientifically robust evidence generation activities are integrated into the project (e.g., innovative approaches such as methods, models, and techniques to achieve claims and end points).
  • Deliver key evidence supporting product claims and registration.
  • Collaborate and integrate expertise from clinical research and Medical Affairs to incorporate clinical endpoints, comparators, healthcare use, and PRO endpoints within the statistical aspects of clinical development protocols which are aligned with evidence requirements and project evidence plan.
  • Research, identify and summarize outsourcing opportunities to support the business objectives.
  • Collaborate with cross-functional R&D stakeholders to implement an outsourcing strategy and select suitable vendors to support evidence generation by the MA&EG team. • Assist in efforts to identify, integrate, and/or develop valid clinical outcome assessments (PRO/COA) measurements for use in clinical programs.




Compliance and adherence to SOPs: 

  • Compliance with necessary regulations for quality and disclosure.
  • Ensure the clinical standard operating procedures are regularly reviewed, implemented, and adhered to.
  • Input into and ownership of relevant standard operating procedures.
  • Ensure best practices and consistency within the team. 

Governance of vendors: 

  • Optimise outsourcing of activities associated with evidence generation, including support to other Evidence Generation& Clinical Research teams taking into account costs, quality, and time constraints. 
  • Evaluate performance of vendors.
  • Attend governance meetings with (preferred) vendors across studies.

Key Challenges:

  • Influencing multiple stakeholders in a matrix organisation using and presenting statistics and outsourcing concepts in layman’s terms.
  • Risk based approach to the delegation of responsibilities to external vendors, maintaining accountability for oversight.
  • Effective time-management to achieve optimal balance between gaining insight, generating high value evidence, and maintaining oversight.
  • Ensuring pre-agreed timelines are met with quality.
  • Managing conflicting priorities between project activities with evolving and often challenging timelines.
  • Creating and maintaining good working relationships with external vendors.


Skills & experience required:

  • Significant statistical knowledge and experience in a Consumer Healthcare environment or similar around design and execution of clinical studies understanding the regulatory environment to be able to deliver appropriately.
  • An external focus and development mindset to ensure a knowledge and understanding of recent developments technically, pertaining to regulatory requirements and competitor activity and products.


You’ll love it because… 
…you’ll get to make an impact like never before. You’ll be responsible for your own projects - we can’t wait to hear your ideas. The products you help us get out there will make people’s lives better. Our iconic brands will provide an incredible platform for you. And our dynamic, ownership-driven culture will help bring the very best out of you, every day.



All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion; 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: Clinical Research, Medical Research, Healthcare

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