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 outcomes

• 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)

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.

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

• Strong Analytical Skills
• Attention To Detail

• German AMNOG Process
• IQWiG Methodology
• G-BA Procedures