> Markdown version of [/jobs/ext/3594227-senior-statistical-programmer](https://www.wearedevelopers.com/jobs/ext/3594227-senior-statistical-programmer). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Senior Statistical Programmer - **Company:** ICon GmbH & Co. KG - **Location:** Frankfurt am Main, Germany - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Clinical Data Repository, R (Programming Language), Macros, Information Technology - **Published:** October 6, 2026 - **Apply:** https://www.jobfinder.de/job/senior-statistical-programmer/ ## About the Role Sciences, or a related quantitative field, Experience in statistical programming within a clinical research, biotechnology, or pharmaceutical environment.Strong proficiency in R programming, including the development and validation of clinical trial datasets, analyses, and reporting outputs.Good understanding of CDISC standards, including SDTM and ADaM, and their application within clinical trials.Familiarity with regulatory requirements and industry guidance related to statistical programming and clinical data reporting.Excellent analytical and problem-solving skills, with a keen attention to detail.Strong communication skills, with the ability to work collaboratively in a team environment and effectively convey complex information.Employment with ICON is contingent upon having the legal right to work in the country where the role is based.Rewards & BenefitsICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career ## Description Statistical Programming team to create, validate and generate statistical outputs, including listings, tables, figures, and CDISC-compliant SDTM and ADaM datasets (including mapping specifications) of low to moderate complexity.Collaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data.Performing quality control and validation of statistical outputs, ensuring accuracy, consistency, and regulatory compliance.Assisting in the preparation of statistical reports, presentations, and publications to support regulatory submissions and clinical study reporting.Contributing to process improvements by identifying efficiencies in programming practices, automation, and the use of R-based analytical workflows.Supporting the development, maintenance, and enhancement of standardized R programming tools, macros, and reporting solutions across studies.Your Profile, Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, Life