HTA Programmer: Biostatistics & AMNOG Analytics

Deutsche Telekom; La Coruña; Híbrido; EUR 55.000 - 90.000; Jornada completa

Descripción de la vacante

IQVIA in Madrid, Spain seeks a Programmer (SAS & R) with German to support health technology assessment and market access activities in Germany. The role centers on statistical programming and analysis of clinical trial data.

You will collaborate with cross-functional teams, contribute to German AMNOG dossiers, and apply CDISC SDTM/ADaM standards. Fluent German and English required; HTA/HEOR experience is a plus.

Formación

• Master's degree or PhD in biostatistics, data science or related field.
• Initial HTA, AMNOG, HEOR or Market Access experience preferred.
• Solid understanding of clinical study designs and endpoints.
• Familiarity with clinical study data standards (CDISC SDTM/ADaM).
• Familiarity with the German AMNOG processes is a plus.

Responsabilidades

• 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

Conocimientos

SAS programming

R programming

German language

English language

Analytical skills

Data science

Educación

Master's degree in Biostatistics or Data Science

PhD in a related field

Herramientas

CDISC SDTM/ADaM

Descripción del empleo

IQVIA in Madrid, Spain seeks a Programmer (SAS & R) with German to support health technology assessment and market access activities in Germany. The role centers on statistical programming and analysis of clinical trial data.

You will collaborate with cross-functional teams, contribute to German AMNOG dossiers, and apply CDISC SDTM/ADaM standards. Fluent German and English required; HTA/HEOR experience is a plus.