Contract Statistical Programmer

We are supporting a global pharmaceutical organisation in the search for an experienced Statistical Programmer to join a specialist biometrics function on a contract basis for 12 months initially.

This role will focus on supporting independent statistical and safety analysis activities across clinical development programmes, working closely with statisticians and cross-functional study teams.

Key Responsibilities

• Deliver statistical programming support for clinical trial analysis and reporting activities
• Develop and validate datasets, tables, listings, and figures (TLFs)
• Support independent safety and statistical analysis workstreams
• Collaborate with biostatistics and clinical teams to ensure high-quality deliverables
• Contribute to programming standards, QC processes, and regulatory compliance activities

Required Experience

• Strong hands-on experience with SAS programming
• Experience using R within a clinical research or pharmaceutical environment
• Background in statistics, biostatistics, or statistical programming
• Experience supporting clinical trial analysis within biotech/pharma/CRO settings
• Understanding of clinical data standards and reporting requirements

Desirable

• Experience supporting safety analyses or independent statistical review activities
• Familiarity with regulatory submission environments
• Previous experience working within global clinical development teams