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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Programmer (SAS & R) with German - Spain-based (remote/hybrid) - **Company:** IQVIA - **Location:** Madrid, Spain (Remote available) - **Contract:** Permanent contract - **Skills:** Clinical Data Repository, Computer Programming, R (Programming Language), SAS (Software) - **Published:** September 16, 2026 - **Apply:** https://dejobs.org/x/x/D5B77214087748A48CCE0AB0BC948F3A/job/ ## About the Role * Master's degree or PhD in biostatistics, data science , or a related field * Initial experience in HTA, AMNOG, HEOR, or Market Access (industry, consultancy, or research institute preferred) and/or in clinical development * Solid understanding of clinical study designs, endpoints, and statistical principles * Familiarity with clinical study data and the corresponding industry standards (CDISC SDTM/ADaM) * Familiarity with the German AMNOG process , IQWiG methodology, or G-BA procedures is an advantage, * Strong analytical skills and attention to detail * Ability to translate complex data into clear and structured output * Affinity for data and excellent analytical and conceptual skills * Strong background in statistics/data sciences/programming with a focus on process automation * 2 years experience in advanced SAS programming , R programming skills are an advantage * 2 years hands-on clinical data analysis experience with CDISC SDTM/ADaM datasets * Solid understanding of core statistical methods used in clinical trials and HEOR Personal Competencies * Structured, reliable, and quality-driven working style * Strong teamwork and communication skills * Fluent German and English , written and spoken (this is an absolute must) * Strong strategic and critical thinking skills focus on quality, service, and solutions. * Well-organized, highly independent, highly motivated * Strong customer orientation, a high level of responsibility and reliability * High attention to detail, and audit-ready mindset ## Description * Contribute to the development of German AMNOG dossiers, with a focus on programming of statistical analyses for Module 4 * Perform scientific assessment and analysis of clinical trial data, including analysis of efficacy, safety, patient-relevant endpoints, and subgroup analyses * Perform meta-analyses and indirect treatment comparisons and support interpretation of statistical outputs * Contribute to the automation and standardization of analysis workflows to ensure efficiency, consistency, and reproducibility * Collaborate closely with cross functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team) * Ensure scientific quality, clarity, and consistency of generated outcomes * Monitor and interpret methodological developments from IQWiG, G BA, and relevant HTA bodies ## Related Videos - [Photonic Computing: Programming a New Class of AI Accelerators (incl. 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