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Programmer (SAS & R) with German - Spain-based (remote/hybrid)
Madrid, Spain

Madrid, Spain

Full time

R

Key Responsibilities:

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- Contribute to the development of German AMNOG dossiers, with a focus on programming of statistical analyses for Module 4
- Perform scientific assessment and analysis of clinical trial data, including analysis of efficacy, safety, patient‑relevant endpoints, and subgroup analyses
- Perform meta‑analyses and indirect treatment comparisons and support interpretation of statistical outputs
- Contribute to the automation and standardization of analysis workflows to ensure efficiency, consistency, and reproducibility
- Collaborate closely with cross functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team)
- Ensure scientific quality, clarity, and consistency of generated outcomes
- Monitor and interpret methodological developments from IQWiG, G BA, and relevant HTA bodies

Your Profile:





Education & Technical Background

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- 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

Skills

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- Strong analytical skills and attention to detail
- Ability to translate complex data into clear and structured output
- Affinity for data and excellent analytical and conceptual skills
- Strong background in statistics/data sciences/programming with a focus on process automation
- >2 years experience in advanced SAS programming , R programming skills a

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