Rrhh Administrativo Bilingüe En/Ch – Gestión Internacional
Hace 2 días
Madrid, España
Aldesa
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Programmer (SAS & R) with German
- Spain-based (remote/hybrid)Madrid, SpainMadrid, SpainFull timeRWe are looking for a highly motivated HTA Programmer (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for biostatisticians or data scientists with a strong interest in applying clinical evidence to reimbursement and market access decision-making. A substantial part of the role involves statistical programming .
Key Responsibilities
+ Contribute to the development of German AMNOG dossiers, with a focus on programming of statistical analyses for Module 4+ Perform scientific assessment and analysis of clinical trial data, including analysis of efficacy, safety, patient-relevant endpoints, and subgroup analyses+ Perform meta-analyses and indirect treatment comparisons and support interpretation of statistical outputs+ Contribute to the automation and standardization of analysis workflows to ensure efficiency, consistency, and reproducibility+ Collaborate closely with cross functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team)+ Ensure scientific quality, clarity, and consistency of generated outcomes+ Monitor and interpret methodological developments from IQWiG, G BA, and relevant HTA bodies
Your Profile
Education & Technical Background+ Master's degree or PhD in **biostatistics, data science
- Spain-based (remote/hybrid)Madrid, SpainMadrid, SpainFull timeRWe are looking for a highly motivated HTA Programmer (Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited for biostatisticians or data scientists with a strong interest in applying clinical evidence to reimbursement and market access decision-making. A substantial part of the role involves statistical programming .
Key Responsibilities
+ Contribute to the development of German AMNOG dossiers, with a focus on programming of statistical analyses for Module 4+ Perform scientific assessment and analysis of clinical trial data, including analysis of efficacy, safety, patient-relevant endpoints, and subgroup analyses+ Perform meta-analyses and indirect treatment comparisons and support interpretation of statistical outputs+ Contribute to the automation and standardization of analysis workflows to ensure efficiency, consistency, and reproducibility+ Collaborate closely with cross functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team)+ Ensure scientific quality, clarity, and consistency of generated outcomes+ Monitor and interpret methodological developments from IQWiG, G BA, and relevant HTA bodies
Your Profile
Education & Technical Background+ Master's degree or PhD in **biostatistics, data science