Programador HTA (R/SAS) – Remoto/Híbrido

Elpuertodesantamaria; Albacete; Híbrido; EUR 42.000 - 65.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Programmer (SAS & R) with German to support health technology assessment and market access activities for Germany, based in Spain with remote/hybrid options. The role targets biostatisticians or data scientists focused on applying clinical evidence to reimbursement decisions.

You will contribute to AMNOG dossiers, perform analyses of clinical trial data, and help automate analysis workflows.

Formación

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

Responsabilidades

• Contribute to the development of German AMNOG dossiers, focusing on statistical analyses for Module 4.
• Analyze clinical trial data for efficacy, safety, endpoints, and subgroup analyses.
• Perform meta-analyses and indirect treatment comparisons; 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 relevant HTA bodies.

Conocimientos

Analytical thinking

Data interpretation

Process automation

Teamwork

Communication

Educación

Master's or PhD in biostatistics/data science

Herramientas

SAS

R

CDISC SDTM/ADaM

Descripción del empleo

IQVIA is seeking a Programmer (SAS & R) with German to support health technology assessment and market access activities for Germany, based in Spain with remote/hybrid options. The role targets biostatisticians or data scientists focused on applying clinical evidence to reimbursement decisions.

You will contribute to AMNOG dossiers, perform analyses of clinical trial data, and help automate analysis workflows.