HTA Programmer – Biostatistics (Remote/Hybrid, Germany)

Empresa De Gestión Y Selección

España

Hybrid

EUR 45,000 - 65,000

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 for AMNOG dossiers, HEOR analyses, and market access support.

Ideal candidates are biostatisticians or data scientists with SAS >2 years and some R experience, fluent German and English, and a solid understanding of clinical study design and CDISC SDTM/ADaM. The position involves developing analyses for Module 4, automating workflows, and collaborating with

Qualifications

  • Master's 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 German AMNOG processes and IQWiG/G-BA procedures is a plus.

Responsibilities

  • Develop statistical analyses for German AMNOG dossiers (Module 4).
  • Analyze clinical trial data, including efficacy, safety, endpoints, and subgroups.
  • Perform meta-analyses and indirect treatment comparisons.
  • Automate and standardize analysis workflows for efficiency and reproducibility.
  • Collaborate with Market Access, HEOR, Medical Affairs, EU-HTA teams.

Skills

Analytical skills
Data interpretation
Statistics / data science
SAS programming
R programming
CDISC SDTM/ADaM
Process automation
German language
English language

Education

Master's degree in biostatistics / data science
PhD in related field
HTA / AMNOG / HEOR / Market Access experience

Tools

CDISC SDTM/ADaM

Job description

IQVIA in Madrid, Spain is seeking a Programmer (SAS & R) with German for remote/hybrid work. The role focuses on statistical programming for AMNOG dossiers, HEOR analyses, and market access support.

Ideal candidates are biostatisticians or data scientists with SAS >2 years and some R experience, fluent German and English, and a solid understanding of clinical study design and CDISC SDTM/ADaM. The position involves developing analyses for Module 4, automating workflows, and collaborating with

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