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Veramed

Senior/Principal Statistician

🗓️ Posted 2026-09-22 Poland; United Kingdom Hybrid Science Technology

Company shared salary

NA

Market rate

4,500 GBP–8,000 GBP/mo (54,000 GBP–96,000 GBP/yr)

Based on similar roles (title + domain + location).

About the Company

We are looking for Senior and Principal Statisticians in the UK and Poland to join Veramed, where you'll deliver high-impact statistics solutions in an FSP-style capacity, while advancing your career in a supportive, growth-driven environment. At Veramed, we focus on two key areas: providing exceptional statistical and programming consultancy, and fostering a workplace where our employees can thrive. We're committed to helping you achieve your unique career goals through tailored development opportunities. We offer office based, hybrid and remote opportunities.

About the Role

The purpose of this role is to provide high quality statistical support. As a Senior Statistician, you may also take on a supervisory role, including line management and/or project leadership, depending on experience and interest. This role is well suited to someone with significant experience in clinical studies and regulatory submissions, who is comfortable working directly with clients. You will be confident working independently, managing your own workload, and contributing across multiple projects and clients. Strong communication skills are essential, including the ability to explain statistical concepts to non statisticians and to present clearly and confidently to client teams.

Responsibilities

  • ● Statistical oversight at study level
  • ● Providing project level statistical input across clinical studies
  • ● Review and oversight of statistical deliverables from other CROs
  • ● Development and/or review of study documentation, including statistical sections of protocols and Statistical Analysis Plans (SAPs)
  • ● Study design activities, including sample size calculations, ad hoc and exploratory analyses
  • ● Additional statistical support as required across client projects
  • ● Confident coding in R, SAS, or other non SAS languages (or a willingness to learn)

Requirements

  • ● Senior level (4+ years) experience in statistics within a clinical research environment.
  • ● Experience working on clinical studies and regulatory submissions.
  • ● Comfortable working independently with clients, often without in house statistical support.
  • ● Strong communication skills and the ability to explain statistical concepts to non statisticians.
  • ● Curious, proactive, and motivated to continuously learn and improve.
  • ● Presenting at conferences and authoring publications.
  • ● Developing and implementing innovative statistical methodologies, study designs, and efficiency optimisation ideas.
  • ● Line management and peer mentoring opportunities.
  • ● Contributing to business process improvements and internal training.
  • ● Supporting initiatives linked to employees, the environment, and local communities as part of our B Corp accreditation.
  • ● A warm, friendly working environment where you can thrive both personally and professionally.
  • ● Supportive, open door management that actively encourages development
  • ● Exposure to a wide variety of clients and projects, including collaboration with leading global pharmaceutical companies.
  • ● The opportunity to work with a truly unique CRO that does things differently - valuing people, relationships, and quality.
  • ● The chance to genuinely own your role and shape your career path.