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# Biostatistician, Sas, R - German Hta Submissions

- **Company:** Jobtailor
- **Location:** Barcelona, Spain
- **Contract:** Permanent contract
- **Skills:** Clinical Data Management, SAS (Software)
- **Published:** October 11, 2026
- **Apply:** https://www.buscojobs.com.es/biostatistician-sas-r-german-hta-submissions-en-barcelona-ID-374363488

## About the Role

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 outcomesRequirements- 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
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 Skills- Statistical Analysis- Meta-Analysis- Clinical Trial Data Assessment- Automation Of Analysis Workflows- Indirect Treatment ComparisonsSoft Skills- Strong Analytical Skills- Attention To DetailIndustry Keywords- German AMNOG Process- IQWiG Methodology- G-BA Procedures#J-*****-Ljbffr

## Description

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 outcomesRequirements- 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 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 Skills- Statistical Analysis- Meta-Analysis- Clinical Trial Data Assessment- Automation Of Analysis Workflows- Indirect Treatment ComparisonsSoft Skills- Strong Analytical Skills- Attention To DetailIndustry Keywords- German AMNOG Process- IQWiG Methodology- G-BA Procedures#J-*****-Ljbffr