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

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