Health Technology Assessment Consultant with German - Working from Spain (hybrid or home-based)

Overview

As an HTA Analyst / Consultant, you will support German AMNOG dossiers and market access activities from Spain, translating clinical evidence into reimbursement decisions. You will perform data-driven scientific assessments, author medical writing deliverables, and collaborate with cross-functional teams to ensure high-quality HTA documents. The role emphasizes German AMNOG expertise, statistical literacy, and medical writing, with impact on market access decisions.

This is a chance to shape dossiers and influence payer-facing communications within a global team.

• Contribute to the development of German AMNOG dossiers (Modules 2–4)
• Perform scientific assessment of trial data including efficacy, safety, endpoints, and subgroup analyses
• Conduct systematic literature reviews and structured evidence syntheses
• Medical writing for AMNOG dossier texts, updates, statements for G BA procedures, scientific reports and slides
• Support indirect treatment comparisons and interpretation of statistical outputs
• Collaborate with cross-functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team)
• Ensure scientific quality, clarity, and consistency of HTA-related documents
• Monitor methodological developments from IQWiG, G BA, and relevant HTA bodies

• Master’s degree or PhD in life sciences, biostatistics, epidemiology, pharmacy, or related field
• Initial HTA/AMNOG/HEOR or Market Access experience (industry, consultancy, or research institute)
• Solid understanding of clinical study designs, endpoints, and statistical principles
• Familiarity with German AMNOG process, IQWiG methodology, or G‑BA procedures is an advantage
• Experience in scientific and medical writing
• Strong analytical skills and attention to detail; ability to translate data into clear text
• Experience in data analysis (advanced Excel); familiarity with Python is a plus
• Strong background in statistics/data sciences/programming;
• 2+ years SAS and R programming experience
• 2+ years clinical data analysis with CDISC SDTM/ADaM datasets
• Proficiency in MS Office; reference management tools a plus
• Fluent German and English (written and spoken)
• Location flexibility to work from Spain (Madrid/Barcelona)
• Submit CV in English

• Structured and reliable working style
• Strong teamwork and communication
• Strategic and critical thinking with focus on quality
• SAS (2+ years)
• R programming (2+ years)
• CDISC SDTM/ADaM