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




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
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

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