Remote HTA Programmer (SAS & R) - German Market Access

Elpuertodesantamaria; Murcia; Híbrido; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

Elpuertodesantamaria in Madrid, Spain, is seeking a Programmer (SAS & R) with German to support health technology assessment and market access activities in Germany. The role emphasizes statistical programming and analysis for HTA dossiers in a remote/hybrid, full‑time capacity.

You will develop German AMNOG analyses (Module 4), analyze trial data for efficacy and safety, perform meta-analyses, automate workflows, and collaborate with cross‑functional teams (Market Access, HEOR, Medical Affairs,

Formación

• Master's or PhD in biostatistics, data science, or related field.
• HTA/AMNOG/HEOR or Market Access experience preferred.
• Solid understanding of clinical study designs and endpoints.
• Familiarity with CDISC SDTM/ADaM standards.
• Knowledge of German AMNOG/IQWiG/G‑BA is a plus.

Responsabilidades

• Develop German AMNOG dossiers with statistical analyses for Module 4.
• Analyze trial data for efficacy, safety, endpoints and subgroup analyses.
• Perform meta-analyses and indirect treatment comparisons.
• Automate and standardize analysis workflows for efficiency and reproducibility.
• Collaborate with Market Access, HEOR, Medical Affairs, EU-HTA Team.
• Ensure scientific quality and clarity of generated outcomes.
• Monitor methodological developments from IQWiG, G‑BA, and related bodies.

Conocimientos

SAS programming

R programming

CDISC SDTM/ADaM

Statistical analysis

Automation

HTA knowledge

Educación

Master's degree in biostatistics

PhD in biostatistics or data science

Herramientas

SAS

R

Descripción del empleo

Elpuertodesantamaria in Madrid, Spain, is seeking a Programmer (SAS & R) with German to support health technology assessment and market access activities in Germany. The role emphasizes statistical programming and analysis for HTA dossiers in a remote/hybrid, full‑time capacity.

You will develop German AMNOG analyses (Module 4), analyze trial data for efficacy and safety, perform meta-analyses, automate workflows, and collaborate with cross‑functional teams (Market Access, HEOR, Medical Affairs,