Ai Content Optimization Specialist Ii
Hace 2 días
Madrid, España
Relx Inc
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Programmer (SAS & R) with German
- Spain-based (remote/hybrid)Madrid, SpainMadrid, SpainFull timeRWe are looking for a highly motivatedHTA Programmer(Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited forbiostatisticiansordata scientistswith a strong interest in applying clinical evidence to reimbursement and market access decision-making. A substantial part of the role involvesstatistical programming .
Key Responsibilities
Contribute to the development of German AMNOG dossiers, with a focus on programming of statistical analyses for Module 4Perform scientific assessment and analysis of clinical trial data, including analysis of efficacy, safety, patient-relevant endpoints, and subgroup analysesPerform meta-analyses and indirect treatment comparisons and support interpretation of statistical outputsContribute to the automation and standardization of analysis workflows to ensure efficiency, consistency, and reproducibilityCollaborate closely with cross functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team)Ensure scientific quality, clarity, and consistency of generated outcomesMonitor and interpret methodological developments from IQWiG, G BA, and relevant HTA bodiesYour Profile:Education & Technical BackgroundMaster's degree or PhD inbiostatistics, data science, or a related field
- Spain-based (remote/hybrid)Madrid, SpainMadrid, SpainFull timeRWe are looking for a highly motivatedHTA Programmer(Analyst/Consultant) to support health technology assessment (AMNOG) and market access activities in Germany. The role is ideally suited forbiostatisticiansordata scientistswith a strong interest in applying clinical evidence to reimbursement and market access decision-making. A substantial part of the role involvesstatistical programming .
Key Responsibilities
Contribute to the development of German AMNOG dossiers, with a focus on programming of statistical analyses for Module 4Perform scientific assessment and analysis of clinical trial data, including analysis of efficacy, safety, patient-relevant endpoints, and subgroup analysesPerform meta-analyses and indirect treatment comparisons and support interpretation of statistical outputsContribute to the automation and standardization of analysis workflows to ensure efficiency, consistency, and reproducibilityCollaborate closely with cross functional teams (Market Access, HEOR, Medical Affairs, EU-HTA Team)Ensure scientific quality, clarity, and consistency of generated outcomesMonitor and interpret methodological developments from IQWiG, G BA, and relevant HTA bodiesYour Profile:Education & Technical BackgroundMaster's degree or PhD inbiostatistics, data science, or a related field