A global clinical research organisation is seeking an experienced Senior Statistical Programmer to support complex clinical studies and deliver high-quality statistical programming solutions across global research projects.

This role is ideal for professionals with strong SAS programming expertise, clinical trial experience, and the ability to lead programming activities across multiple studies within a fast-paced CRO or pharmaceutical environment.

Key Responsibilities

• Develop, test, validate, and maintain statistical programs for clinical trial analysis and reporting
• Create analysis datasets, tables, listings, and figures (TLFs) for complex studies
• Integrate and manage datasets from multiple studies and sources
• Lead programming activities for individual studies or portfolios of studies
• Develop programming specifications, documentation, and validation plans
• Support database quality control and d...