We are currently looking for an experienced Biostatistician to join a leading consultancy on an initial 3-month contract (Possibility of Extension).

This role will involve supporting Phase I–IV clinical studies through statistical analysis, reporting, and interpretation of clinical trial data. You’ll work closely with cross‑functional teams to help deliver high‑quality statistical outputs within a regulated environment.

Key responsibilities include:

• Preparing statistical analysis plans and study outputs
• Performing analysis of clinical trial data
• Supporting study reporting and interpretation of results
• Contributing to the timely delivery of clinical development activities

To be considered, you should have:

• An MSc in Biostatistics, Statistics, or a related discipline
• Previous experience within pharma, biotech, or CRO settings
• Strong SAS programming experienc...