Programmer With German Language - German Hta Submissions - Spain-Based (Remote/Hybrid)

IQVIA
Barcelona, Spain
15 days ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English, German

Tech stack

Data Analysis Clinical Data Management Clinical Data Repository Computer Programming R (Programming Language) SAS (Software)

Job description

About IQVIADé el siguiente paso en su carrera profesional ahora: desplácese hacia abajo para leer la descripción completa del puesto y envíe su solicitud.IQVIA is a fast-growing and highly successful business, delivering data-driven insights and measurable impact for clients across the global life sciences ecosystem.Leveraging access to some of the world’s most comprehensive healthcare data, advanced analytics and research capabilities, IQVIA experts design and deliver innovative, technology-enabled evidence programs to support decision-making across the product lifecycle.Job DescriptionWe are looking for a highly motivated HTA Analyst-Programmer 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 ResponsibilitiesContribute 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 bodiesEducation & Technical BackgroundMaster’s degree or PhD in biostatistics, data science, or a related fieldInitial experience in HTA, AMNOG, HEOR, or Market Access (industry, consultancy, or research institute preferred) and/or in clinical developmentSolid understanding of clinical study designs, endpoints, and statistical principlesFamiliarity with clinical study data and the corresponding industry standards (CDISC SDTM/ADaM)Familiarity with the German AMNOG process, IQWiG methodology, or G?BA procedures is an advantageSkillsStrong analytical skills and attention to detailAbility to translate complex data into clear and structured outputAffinity for data and excellent analytical and conceptual skillsStrong background in statistics/data sciences/programming with a focus on process automation2 or more years experience in advanced SAS programming; R programming skills are an advantage2 or more years hands?on clinical data analysis experience with CDISC SDTM/ADaM datasetsSolid understanding of core statistical methods used in clinical trials and HEORPersonal CompetenciesStructured, reliable, and quality?driven working styleStrong teamwork and communication skillsFluent German and English, written and spoken (this is an absolute must)Strong strategic and critical thinking skills focus on quality, service, and solutionsWell-organized, highly independent, highly motivatedStrong customer orientation, a high level of responsibility and reliabilityHigh attention to detail, and audit-ready mindsetPlease submit your CV in English.xqbhyrx #J-*****-LjbffrHay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

Requirements

Leveraging access to some of the world’s most comprehensive healthcare data, advanced analytics and research capabilities, IQVIA experts design and deliver innovative, technology-enabled evidence programs to support decision-making across the product lifecycle.Job DescriptionWe are looking for a highly motivated HTA Analyst-Programmer 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 ResponsibilitiesContribute 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 bodiesEducation & Technical BackgroundMaster’s degree or PhD in biostatistics, data science, or a related fieldInitial experience in HTA, AMNOG, HEOR, or Market Access (industry, consultancy, or research institute preferred) and/or in clinical developmentSolid understanding of clinical study designs, endpoints, and statistical principlesFamiliarity with clinical study data and the corresponding industry standards (CDISC SDTM/ADaM)Familiarity with the German AMNOG process, IQWiG methodology, or G?BA procedures is an advantageSkillsStrong analytical skills and attention to detailAbility to translate complex data into clear and structured outputAffinity for data and excellent analytical and conceptual skillsStrong background in statistics/data sciences/programming with a focus on process automation2 or more years experience in advanced SAS programming; R programming skills are an advantage2 or more years hands?on clinical data analysis experience with CDISC SDTM/ADaM datasetsSolid understanding of core statistical methods used in clinical trials and HEORPersonal CompetenciesStructured, reliable, and quality?driven working styleStrong teamwork and communication skillsFluent German and English, written and spoken (this is an absolute must)Strong strategic and critical thinking skills focus on quality, service, and solutionsWell-organized, highly independent, highly motivatedStrong customer orientation, a high level of responsibility and reliabilityHigh attention to detail, and audit-ready mindsetPlease submit your CV in English. xqbhyrx #J-*****-LjbffrHay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.

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