Job Description
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 data transfer activities
Build and improve SAS macros, automation ...
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 data transfer activities
Build and improve SAS macros, automation ...