Programmer (SAS & R) with German - Spain based (remote/hybrid)Madrid, SpainFull timeRWe are looking for a highly motivatedHTA Programmer(Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited forbiostatisticiansordata scientistswith a strong interest in applying clinical evidence to reimbursement and market access decision-making. A substantial part of the role involvesstatistical programming .Key ResponsibilitiesContribute to the development of German AMNOG dossiers, with a focus on programming of statistical analyses for Module 4Perform scientific assessment and analysis of clinical trial data, including analysis of efficacy, safety, patient-relevant endpoints, and subgroup analysesPerform meta-analyses and indirect treatment comparisons and support interpretation of statistical outputsContribute to the automation and standardization of analysis workflows to ensure efficiency, consistency, and reproducibilityCollaborate closely with cross functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team)Ensure scientific quality, clarity, and consistency of generated outcomesMonitor and interpret methodological developments from IQWiG, G BA, and relevant HTA bodiesYour ProfileEducation & Technical BackgroundMaster's degree or PhD inbiostatistics, data science, or a related fieldInitial experience inHTA, AMNOG, HEOR, or Market Access(industry, consultancy, or research institute preferred) and/or inclinical developmentSolid understanding ofclinical study designs, endpoints,



and statistical principlesFamiliarity withclinical study dataand the corresponding industry standards (CDISC SDTM/ADaM)Familiarity with theGerman AMNOG process, IQWiG methodology, or G‑BA procedures is an advantageSkillsStronganalytical skillsand attention to detailAbility to translate complex data intoclear and structured outputAffinity for data and excellent analytical and conceptual skillsStrong background instatistics/data sciences/programmingwith a focus onprocess automation> 2 years experience in advancedSAS programming, R programming skills are an advantage> 2 years hands‑on clinical data analysis experience withCDISC SDTM/ADaMdatasetsSolid understanding of core statistical methodsused in clinical trials and HEORPersonal CompetenciesStructured, reliable, and quality‑driven working styleStrong teamwork and communication skillsFluentGerman 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 motivatedStrong customer orientation, a high level of responsibility and reliabilityHigh attention to detail, and audit‑ready mindsetPlease submit your CV in English.Company DescriptionIQVIA is a leading integral provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.EEOEEO Minorities/Females/Protected Veterans/Disabled#J-18808-Ljbffr

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