HTA Programmer (Biostatistics) — Remote/Hybrid

Activando Talento En Acción

Málaga

Hybrid

EUR 48,000 - 72,000

Full time

3 days ago
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Job summary

IQVIA is seeking a Programmer (SAS & R) with German, based in Spain with remote/hybrid work options. The role focuses on health technology assessment and market access for Germany, requiring biostatistics or data science expertise and strong SAS/SDTM/ADaM capabilities.

Ideal candidates combine statistical programming with a deep understanding of HTA processes, AMNOG, and clinical study design. Collaboration with EU-HTA teams and cross-functional groups is essential.

Qualifications

  • Master's or PhD in biostatistics, data science, or a related field.
  • Experience in HTA, AMNOG, HEOR, or Market Access.
  • Strong understanding of clinical study designs and statistics.
  • Familiarity with clinical study data and industry standards (CDISC SDTM/ADaM).
  • Knowledge of German AMNOG process or IQWiG/G-BA is a plus.

Responsibilities

  • Develop German AMNOG dossiers with SAS analyses for Module 4.
  • Analyze trial data for efficacy, safety, endpoints and subgroups.
  • Perform meta-analyses and indirect comparisons and interpret results.
  • Automate and standardize analysis workflows for consistency.
  • Collaborate with Market Access, HEOR, Medical Affairs and EU-HTA teams.
  • Ensure scientific quality, clarity and reproducibility of outputs.
  • Monitor IQWiG, GBA methodologies and HTA guidance.

Skills

SAS programming
R programming
German language
English language
Statistical programming
Data analysis

Education

Master's or PhD in biostatistics or data science

Tools

CDISC SDTM/ADaM

Job description

IQVIA is seeking a Programmer (SAS & R) with German, based in Spain with remote/hybrid work options. The role focuses on health technology assessment and market access for Germany, requiring biostatistics or data science expertise and strong SAS/SDTM/ADaM capabilities.

Ideal candidates combine statistical programming with a deep understanding of HTA processes, AMNOG, and clinical study design. Collaboration with EU-HTA teams and cross-functional groups is essential.

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