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