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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 ProfileEducation & Technical BackgroundMaster's degree or PhD inbiostatistics, data science, or a related fieldInitial experience inHTA, AMNOG, HEOR, or Market Access(industry, consultancy, or research institute preferred) and/or inclinical developmentSolid understanding ofclinical study designs, endpoints, and statistical principlesFamiliarity withclinical study dataand the corresponding industry standards (CDISC SDTM/ADaM)Familiarity with theGerman AMNOG process, IQWiG methodology, or G‑BA procedures is an advantageSkillsStronganalytical skillsand attention to detailAbility to translate complex data intoclear and structured outputAffinity for data and excellent analytical and conceptual skillsStrong background instatistics/data sciences/programmingwith a focus onprocess automation> 2 years experience in advancedSAS programming, R programming skills are an advantage> 2 years hands‑on clinical data analysis experience withCDISC SDTM/ADaMdatasetsSolid understanding of core statistical methodsused in clinical trials and HEORPersonal CompetenciesStructured, reliable, and quality‑driven working styleStrong teamwork and communication skillsFluentGerman and English, written and spoken(this is an absolute must)Strong strategic and critical thinking skills focus on quality, service, and solutions.
Well-organized, highly independent, highly motivatedStrong customer orientation, a high level of responsibility and reliabilityHigh attention to detail, and audit-ready mindsetIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at .
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers imp
- 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 ProfileEducation & Technical BackgroundMaster's degree or PhD inbiostatistics, data science, or a related fieldInitial experience inHTA, AMNOG, HEOR, or Market Access(industry, consultancy, or research institute preferred) and/or inclinical developmentSolid understanding ofclinical study designs, endpoints, and statistical principlesFamiliarity withclinical study dataand the corresponding industry standards (CDISC SDTM/ADaM)Familiarity with theGerman AMNOG process, IQWiG methodology, or G‑BA procedures is an advantageSkillsStronganalytical skillsand attention to detailAbility to translate complex data intoclear and structured outputAffinity for data and excellent analytical and conceptual skillsStrong background instatistics/data sciences/programmingwith a focus onprocess automation> 2 years experience in advancedSAS programming, R programming skills are an advantage> 2 years hands‑on clinical data analysis experience withCDISC SDTM/ADaMdatasetsSolid understanding of core statistical methodsused in clinical trials and HEORPersonal CompetenciesStructured, reliable, and quality‑driven working styleStrong teamwork and communication skillsFluentGerman and English, written and spoken(this is an absolute must)Strong strategic and critical thinking skills focus on quality, service, and solutions.
Well-organized, highly independent, highly motivatedStrong customer orientation, a high level of responsibility and reliabilityHigh attention to detail, and audit-ready mindsetIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at .
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers imp