Senior/Principal Statistician

Veramed prides itself on two key areas: providing the highest quality statistical and programming consultancy to our clients, and offering our employees an industry‑leading working environment with outstanding support, training, and opportunities for career growth. We have an exciting opportunity for a Senior to Principal level Statistician to join us on a permanent basis. We offer flexible working (home, hybrid or office‑based), structured training and development, and a competitive package.

The Role

The purpose of this role is to provide high‑quality statistical support to one of our key FSP clients. As a Senior or Principal 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 - including situations where there is no internal statistical support. 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.

Key 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)

Experience & Skills

Essential:

Senior to Principal level 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

Desirable:

Study design and sample size experience

Regulatory experience