Analista Programador HTA (SAS/R) – Alemán

Líder En Moda De Alta Costura

Talavera de la Reina

Hybrid

EUR 60,000 - 80,000

Full time

2 days ago
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Job summary

IQVIA in Madrid, Spain is seeking a Programmer (SAS & R) with German for remote/hybrid work. The role focuses on statistical programming to support health technology assessment and market access activities in Germany, ideal for biostatisticians or data scientists.

You will develop German AMNOG dossiers, analyze trial data, automate workflows, and collaborate with Market Access, HEOR, Medical Affairs, and EU-HTA teams while staying abreast of IQWiG and G-BA guidelines.

Qualifications

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

Responsibilities

  • Develop German AMNOG dossiers focusing on Module 4 analyses.
  • Analyze clinical trial data for efficacy, safety, endpoints.
  • Perform meta-analyses and indirect comparisons.
  • Automate analysis workflows for consistency and efficiency.
  • Collaborate with Market Access, HEOR, Medical Affairs, and EU-HTA teams.
  • Ensure clarity and quality of generated outputs.
  • Track developments from IQWiG, G-BA, and HTA bodies.

Skills

Analytical skills
Data analysis
Process automation
Statistical programming
German language proficiency
English language proficiency
SAS programming
R programming
CDISC SDTM/ADaM knowledge
Biostatistics / data science

Education

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

Tools

SAS
R

Job description

IQVIA in Madrid, Spain is seeking a Programmer (SAS & R) with German for remote/hybrid work. The role focuses on statistical programming to support health technology assessment and market access activities in Germany, ideal for biostatisticians or data scientists.

You will develop German AMNOG dossiers, analyze trial data, automate workflows, and collaborate with Market Access, HEOR, Medical Affairs, and EU-HTA teams while staying abreast of IQWiG and G-BA guidelines.

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