Radiation Protection Lead For Nuclear Decommissioning Hybrid

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.
A substantial part of the role involves statistical programming.
Contribute 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 bodiesKey ResponsibilitiesStatistical programming of clinical trial dataStatistical programming of economic dataDesign and run SQL queriesYour ProfileEducation & Technical Background: Master’s degree or PhD in biostatistics, data science, or a related fieldInitial experience in HTA, AMNOG, HEOR, or Market Access (industry, consultancy, or research institute preferred) and/or in clinical developmentSolid understanding of clinical study designs, endpoints, and statistical principlesFamiliarity 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 advantageSkillsStrong analytical skills and attention to detailAbility to translate complex data into clear and structured outputAffinity for data and excellent analytical and conceptual skillsStrong background in statistics/data sciences/programming with a focus on process automationMore than 2 years experience in advanced SAS programming; R programming skills are an advantageMore than 2 years hands‑on clinical data analysis experience with CDISC SDTM/ADaM datasetsSolid understanding of core statistical methods used in clinical trials and HEORPersonal CompetenciesStructured, reliable, and quality‑driven working styleStrong teamwork and communication skillsFluent German and English, written and spoken (this is an absolute must)Strong strategic and critical thinking skills focus on quality, service, and solutionsWell‑organized, highly independent, highly motivatedStrong customer orientation, high level of responsibility and reliabilityHigh attention to detail, audit‑ready mindsetIQVIA is a leading global 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.
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