3 of 3 Statistical Programmer Jobs

A global pharmaceutical company is currently looking for a Senior Statistical Programmer to join their team on a 12-month temporary contract. Why should you apply? Ideal opportunity for a high calibre Statistical Programmer to join a top-20 global pharmaceutical giant. Fully remote working (with occasional expensed, onsite meetings). Will consider talent from CRO … initial 12-month period. Note - using SAS (or R/Python) + SQL in the pharma industry will be essential for an application to be successful. As a Senior Statistical Programmer, you will work on real world data to deliver high quality analyses that support evidence-based decisions in drug development and patient care. Key Responsibilities Develop and … validate complex analysis datasets from large and diverse data sources Perform statistical analyses and create reports for observational studies using Databricks and SAS Interpret and implement analysis plans in close collaboration with epidemiologists Ensure programming accuracy and compliance by reviewing peer code and outputs Identify and resolve data issues, ensuring robust, high quality results Requirements Strong experience in statistical More ❯

Automation & Tools Statistical Programmer Global Pharma UK remote based About the Role We are looking for a Statistical Programmer in Tools & Automation to join our innovative team and help drive the future of programming and process efficiency in clinical research. This is not a traditional programming role: you will design and implement automation frameworks, develop internal … applications, and build proof-of-concept solutions that enhance scalability, speed, and compliance across projects. Key Responsibilities Develop and maintain automation frameworks and internal tools that streamline statistical programming workflows. Design, prototype, and implement applications that improve efficiency and scalability. Support automation of CDISC-compliant workflows (SDTM, ADaM, TLFs). Collaborate with cross-functional teams to identify opportunities for … innovation and process improvement. Maintain and extend statistical computing environments, with integration of SAS, R, and Python-based solutions. Drive continuous improvement through documentation, knowledge sharing, and best practice adoption. What We’re Looking For 8+ years of experience in SAS programming, with proven expertise in CDISC standards (SDTM, ADaM, TLFs). Strong interest and demonstrated ability in automation More ❯

Tech Observer is hiring Senior Statistical Programmers and Principal Programmers in UK and Europe on FSP. Job Responsibilities (But not limited to) Carry out all activities according to Tech Observer SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP). Ensure adherence to programming guidelines. Implement and follow the latest versions of … CDISC, FDA Guidelines, GCP and other industry standards; Participate in and co-ordinate the Statistical Programming review of Case Report Forms (CRFs), annotated CRFs, database structures and study related documentation (e.g. data validation guidelines). Review and interpret Report and Analysis Plans and provide comments for assigned projects. Develop and review SAS programs and output for the management of … clinical trial data, the tabulation of data, preparation of patient data listings, graphical output, and creation of derived datasets and statistical analysis of data as specified in the Statistical or Report Analysis Plans. Develop SAS programs for ad hoc tables and listings. Write, modify, and maintain programs that produce diagnostics and listing for data review in support of More ❯