Programmer (SAS & R) with German - Spain-based (remote/hybrid) Madrid, Spain Full time We are looking for a highly motivated HTA Programmer (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany.

The role is ideally suited for biostatisticians or data scientists with a strong interest in applying clinical evidence to reimbursement and market access decision‑making. A substantial part of the role involves statistical programming.

Key Responsibilities: * 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 Your Profile: Education & Technical Background * 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 Skills * 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 EEO Minorities/Females/Protected Veterans/Disabled #J-18808-Ljbffr

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