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
J-18808-Ljbffr

📌 Biostatistician, SAS, R (España)
🏢 Jobtailor
📍 España