Llm-Interoperabilitätsarchitekt - Komplexe Systemintegration (Hybrid) - Deutsche Telekom

Deutsche Telekom
A Coruña, Spain
1 day ago
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Role details

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

Tech stack

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

Job description

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 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 automation> 2 years experience in advanced SAS programming, R programming skills are an advantage> 2 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 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 improve the lives of patients everywhere.Thank you for your interest in growing your career with us.EEO Minorities/Females/Protected Veterans/Disabled

Requirements

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 automation> 2 years experience in advanced SAS programming, R programming skills are an advantage> 2 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

About the company

(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 improve the lives of patients everywhere. Thank you for your interest in growing your career with us.EEO Minorities/Females/Protected Veterans/Disabled

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