Overview In this SAS Programmer role, you contribute to the clinical data analysis by building analysis datasets, tables, listings, and figures. You will work within the Clinical Database Programming & Biostatistics team to program, validat...Read More>>.

Overview In this role you drive statistical programming for clinical trials, acting as a technical SME and, when needed, leading programming on projects. You collaborate with sponsors and cross-functional teams to ensure quality, timelines,...Read More>>.

A leading global CRO is seeking a Senior Statistical Programmer for a permanent home-based position. The role involves designing data structures, ensuring the quality of clinical data submissions, and leading programming activities across multiple st...Read More>>.

A global clinical research organization in London is inviting applications for a SAS Programmer role. This position requires a Bachelor's degree in relevant fields and SAS Base Certification. Responsibilities include writing SAS programs, validating...Read More>>.

We are looking for a SAS Programmer III who can also program in R with a background in working across clinical trials, ideally with experience in oncology.The successful candidate will be detail-oriented and motivated to deliver high-qualit...Read More>>.

A clinical research organization is looking for a SAS Programmer III with strong SAS and R skills to support clinical trials remotely in the UK. The role involves programming SDTM and ADaM datasets, performing quality control, and collaborating with...Read More>>.

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Job SummaryDue to our continued growth, we are in need of qualified and focused driven individuals for SAS Programmer role to be office-based in Stirling, UK. This is a vital role in our Clinical Database Programming & Biostatistics depar...Read More>>.

Job Overview Responsible for importing, cleaning, transforming, and validating data to ensure its accuracy and integrity for analysis. UsingSAS procedures and functions to perform various statistical analys...Read More>>.

Veramed is seeking a Data Management Programmer to join a sponsor-dedicated team, working as a fully integrated member of a global Data Management Programming function. The role focuses on generating Data Management listings from raw clinical tria...Read More>>.

Veramed is seeking Principal and Senior Statistical Programmers to join a specialist CRO. Roles offer full remote, hybrid or office-based working with a supportive, quality-focused environment.The role provides programming support across pr...Read More>>.

Adelphi Values is recruiting programmers for the PCO Statistics and Programming Team to analyse PRO data from clinical trials and psychometric studies. You will develop SAS programs to generate tables and figures, and improve processes including m...Read More>>.

Veramed in the United Kingdom is seeking a Data Management Programmer to join a sponsor-dedicated team as a fully integrated member of the global Data Management Programming function. The role focuses on generating Data Management listings from ra...Read More>>.

Parexel International is seeking a Senior Statistical Programmer to join our FSP team across the UK, Hungary, Poland, or Serbia. The role involves technical leadership in statistical programming for clinical trials, ensuring quality, timelines, bu...Read More>>.

Parexel is seeking a Senior Statistical (SAS) Programmer to join its FSP team in the UK. The role involves providing technical expertise for clinical trials, leading a global programming team, and supporting sponsors and internal stakeholders on s...Read More>>.

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