Remote HTA Biostatistician & Data Scientist (SAS/R)

Quik Hire Staffing; Burgos; Híbrido; EUR 55.000 - 75.000; Jornada completa

Descripción de la vacante

IQVIA in Madrid, Spain, seeks a Programmer (SAS & R) with German to support health technology assessment (AMNOG) and market access activities for Germany. The role combines statistical programming with clinical data analysis in a remote/hybrid setting.

You will develop German AMNOG dossiers, analyze trial data, run meta-analyses, and collaborate with Market Access, HEOR, Medical Affairs, and the EU-HTA team. A strong background in biostatistics and CDISC SDTM/ADaM is important.

Formación

• Master's degree in biostatistics, data science, or related field.
• Initial HTA/AMNOG/HEOR/Market Access experience preferred.
• Solid understanding of clinical study designs and statistical principles.
• Familiarity with CDISC SDTM/ADaM and German AMNOG processes is a plus.

Responsabilidades

• Contribute to German AMNOG dossiers with a focus on statistical analyses for Module 4.
• Analyse clinical trial data including efficacy, safety, endpoints, and subgroups.
• Perform meta-analyses and indirect treatment comparisons and 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 scientific quality and clarity of generated outcomes.
• Monitor methodological developments from IQWiG, G-BA, and HTA bodies.

Conocimientos

Advanced SAS programming

R programming

Data analysis

Process automation

Attention to detail

Statistics

Educación

Master's degree in biostatistics/data science

Herramientas

SAS

R

CDISC SDTM/ADaM

Descripción del empleo

IQVIA in Madrid, Spain, seeks a Programmer (SAS & R) with German to support health technology assessment (AMNOG) and market access activities for Germany. The role combines statistical programming with clinical data analysis in a remote/hybrid setting.

You will develop German AMNOG dossiers, analyze trial data, run meta-analyses, and collaborate with Market Access, HEOR, Medical Affairs, and the EU-HTA team. A strong background in biostatistics and CDISC SDTM/ADaM is important.