Biostatistician, Sas, R - German Hta Submissions

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

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