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

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

Descripción de la vacante

IQVIA in Madrid, Spain, is seeking a Programmer (SAS & R) with German to support health technology assessment and market access projects for Germany. This full-time role focuses on statistical programming and analysis of clinical trial data.

You will develop German AMNOG dossiers, perform meta-analyses, and collaborate with Market Access, HEOR, and Medical Affairs teams. Fluency in German and English is required, with 2+ years in SAS and CDISC SDTM/ADaM.

Formación

• Master's degree or PhD in biostatistics, data science, or a related field.
• Initial HTA, AMNOG, HEOR, or Market Access experience preferred.
• Solid understanding of clinical study designs and statistical principles.
• Familiarity with German AMNOG, IQWiG, or G-BA procedures is an advantage.

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 efficacy and safety endpoints
• Perform meta-analyses and indirect treatment comparisons and support interpretation of outputs
• Contribute to automation and standardization of analysis workflows for efficiency and reproducibility
• Collaborate with cross functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team)
• Ensure scientific quality and clarity of generated outcomes
• Monitor and interpret methodological developments from IQWiG, G-BA and relevant HTA bodies

Conocimientos

SAS programming

R programming

Clinical data analysis

CDISC SDTM/ADaM

Statistics

Process automation

Educación

Master's degree or PhD in biostatistics, data science, or a related field

Herramientas

CDISC SDTM/ADaM

Descripción del empleo

IQVIA in Madrid, Spain, is seeking a Programmer (SAS & R) with German to support health technology assessment and market access projects for Germany. This full-time role focuses on statistical programming and analysis of clinical trial data.

You will develop German AMNOG dossiers, perform meta-analyses, and collaborate with Market Access, HEOR, and Medical Affairs teams. Fluency in German and English is required, with 2+ years in SAS and CDISC SDTM/ADaM.