Hta Data Scientist (Sas/R) For German Market Access - Remote

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Madrid, Spain
5 days 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)

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 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 standardisation 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 Background Master’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 advantageSkills Strong 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 Competencies Structured, 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 mindsetEEO Statement EEO Minorities/Females/Protected Veterans/Disabled#J-*****-Ljbffr

Requirements

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 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 standardisation 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 Background Master’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 advantageSkills Strong 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 Competencies Structured, 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 mindsetEEO Statement EEO Minorities/Females/Protected Veterans/Disabled#J-*****-Ljbffr

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