Responsibilities

Contribute to the development of German AMNOG dossiers Perform scientific assessment and analysis of clinical trial data Perform meta-analyses and indirect treatment comparisons Contribute to the automation and standardization of analysis workflows Ensure scientific quality, clarity, and consistency of generated outcomes Requirements

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 Fluent German and English,



written and spoken (this is an absolute must) Core Competencies

Demonstrates 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 Skills

Statistical Analysis Meta-Analysis Clinical Trial Data Assessment Automation Of Analysis Workflows Indirect Treatment Comparisons Soft Skills

Strong Analytical Skills Attention To Detail Industry Keywords

German AMNOG Process IQWiG Methodology G-BA Procedures

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📌 Biostatistician, SAS, R – German HTA submissions (Madrid)
🏢 Jobtailor
📍 Madrid