Programador/a HTA (SAS/R) con Alemán – Remoto

Fábrica De Papel De Regalo Y Bolsas De Papel

Brea de Aragón

Hybrid

EUR 50,000 - 90,000

Full time

2 days ago
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Job summary

IQVIA is seeking a Programmer (SAS & R) with German for a Spain-based (remote/hybrid) role to support health technology assessment and market access activities in Germany. The candidate should have a strong background in biostatistics or data science and a keen interest in applying clinical evidence to reimbursement decisions.

The role focuses on statistical programming, analysis of clinical trial data, and collaboration across cross-functional teams.

Qualifications

  • Master's degree or PhD in biostatistics, data science, or a related field.
  • Experience in HTA, AMNOG, HEOR, or Market Access and/or clinical development.
  • Solid understanding of clinical study designs, endpoints, and statistical principles.
  • Familiarity with clinical study data and the CDISC SDTM/ADaM standards.
  • Knowledge of German AMNOG, IQWiG methodology, or G-BA procedures is a plus.

Responsibilities

  • Contribute to German AMNOG dossiers by programming statistical analyses for Module 4.
  • Perform scientific assessment and analysis of clinical trial data, including efficacy and safety.
  • Conduct meta-analyses and indirect comparisons; support interpretation of outputs.
  • Automate and standardize analysis workflows for efficiency and reproducibility.
  • Collaborate with Market Access, HEOR, Medical Affairs, and EU-HTA teams.
  • Ensure clarity and quality of generated outcomes.
  • Monitor IQWiG, GBA, and other HTA methodological developments.

Job description

IQVIA is seeking a Programmer (SAS & R) with German for a Spain-based (remote/hybrid) role to support health technology assessment and market access activities in Germany. The candidate should have a strong background in biostatistics or data science and a keen interest in applying clinical evidence to reimbursement decisions.

The role focuses on statistical programming, analysis of clinical trial data, and collaboration across cross-functional teams.

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