ResponsibilitiesContribute to the development of German AMNOG dossiersPerform scientific assessment and analysis of clinical trial dataPerform meta-analyses and indirect treatment comparisonsContribute to the automation and standardization of analysis workflowsEnsure scientific quality, clarity, and consistency of generated outcomesRequirementsMaster’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 advantageStrong analytical skills and attention to detailFluent German and English,



written and spoken (this is an absolute must)Core CompetenciesDemonstrates expertise in developing German AMNOG dossiers and conducting scientific assessments of clinical trial data, with a strong foundation in biostatistics and data science. Proficient in statistical principles and familiar with industry standards for clinical study data, ensuring high-quality outcomes in health technology assessment.Hard SkillsStatistical AnalysisMeta-AnalysisClinical Trial Data AssessmentAutomation Of Analysis WorkflowsIndirect Treatment ComparisonsSoft SkillsStrong Analytical SkillsAttention To DetailIndustry KeywordsGerman AMNOG ProcessIQWiG MethodologyG-BA Procedures
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📌 Biostatistician, SAS, R – German HTA submissions (Barcelona)
🏢 Jobtailor
📍 Barcelona