HTA Programmer (SAS/R) for German Market – Remote

Barceló Group; Cádiz; Híbrido; EUR 45.000 - 65.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Programmer (SAS & R) with German to support health technology assessment activities in Spain, with remote/hybrid options. The role aligns with biostatisticians or data scientists who excel in statistical programming and applying clinical evidence to reimbursement decisions.

You will contribute to German AMNOG dossiers, analyze trial data for efficacy and safety, and perform meta-analyses while ensuring reproducible workflows. Collaboration with EU-HTA teams is essential.

Formación

• Master's degree or PhD in biostatistics, data science, or related field.
• HTA/AMNOG/HEOR/Market Access experience is preferred.
• Solid understanding of clinical study designs, endpoints, and statistics.
• Familiarity with CDISC SDTM/ADaM data standards.
• German AMNOG processes familiarity is advantageous.

Responsabilidades

• Contribute to the development of German AMNOG dossiers, focusing on programming analyses for Module 4.
• Analyze clinical trial data for efficacy, safety, endpoints, and subgroup analyses.
• Perform meta-analyses and indirect comparisons and support interpretation of outputs.
• Automate and standardize analysis workflows for efficiency, consistency, 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, GBA, and HTA bodies.

Conocimientos

SAS programming

R programming

Statistical analysis

CDISC SDTM/ADaM

HTA/HEOR

Biostatistics

Data science

Educación

Master's or PhD in biostatistics/data science

HTA/AMNOG/HEOR/Market Access experience

Clinical study designs knowledge

CDISC SDTM/ADaM familiarity

Herramientas

SAS

R

Descripción del empleo

IQVIA is seeking a Programmer (SAS & R) with German to support health technology assessment activities in Spain, with remote/hybrid options. The role aligns with biostatisticians or data scientists who excel in statistical programming and applying clinical evidence to reimbursement decisions.

You will contribute to German AMNOG dossiers, analyze trial data for efficacy and safety, and perform meta-analyses while ensuring reproducible workflows. Collaboration with EU-HTA teams is essential.