HTA Data Scientist (SAS/R) for German Market Access

Empresa Tecnologica En Crecimiento; Ciudad Real; Hybrid; EUR 50,000 - 80,000; Full time

Job summary

IQVIA in Spain- based operations seeks a highly motivated HTA Programmer (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities for Germany. The role is suited for biostatisticians or data scientists with a strong interest in applying clinical evidence to reimbursement and decision-making.

A substantial part involves statistical programming. Responsibilities include developing AMNOG dossiers, analyzing trial data, performing meta-analyses, and

Qualifications

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

Responsibilities

• Develop German AMNOG dossiers focusing on programming analyses for Module 4.
• Analyze trial data including efficacy, safety, endpoints, and subgroup analyses.
• Perform meta-analyses and indirect treatment comparisons.
• Automate and standardize 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 methodological developments from IQWiG, G‑BA, and relevant HTA bodies.

Skills

Analytical skills

Data analysis

Programming

Process automation

SAS programming

CDISC SDTM/ADaM

Statistics

Education

Master's degree or PhD in biostatistics or data science

Tools

SAS

R

CDISC SDTM/ADaM

Job description

IQVIA in Spain- based operations seeks a highly motivated HTA Programmer (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities for Germany. The role is suited for biostatisticians or data scientists with a strong interest in applying clinical evidence to reimbursement and decision-making.

A substantial part involves statistical programming. Responsibilities include developing AMNOG dossiers, analyzing trial data, performing meta-analyses, and