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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