Biostatistician, Sas, R - German Hta Submissions

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Madrid, Spain
about 1 month 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

Clinical Data Management SAS (Software)

Job description

ResponsibilitiesContribute to the development of German AMNOG dossiers Perform scientific assessment and analysis of clinical trial data Perform meta-analyses and indirect treatment comparisons Contribute to the automation and standardization of analysis workflows Ensure scientific quality, clarity, and consistency of generated outcomes RequirementsMaster’s degree or PhD in biostatistics, data science, or a related field Initial experience in HTA, AMNOG, HEOR, or Market Access (industry, consultancy, or research institute preferred) and/or in clinical development Solid understanding of clinical study designs, endpoints, and statistical principles Familiarity 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 advantage Strong analytical skills and attention to detail Fluent German and English, written and spoken (this is an absolute must) Core CompetenciesDemonstrates expertise in developing German AMNOG dossiers and conducting scientific assessments of clinical trial data, with a strong foundation in biostatistics and data science.Proficient in statistical principles and familiar with industry standards for clinical study data, ensuring high-quality outcomes in health technology assessment.Hard SkillsStatistical Analysis Meta-Analysis Clinical Trial Data Assessment Automation Of Analysis Workflows Indirect Treatment Comparisons Soft SkillsStrong Analytical Skills Attention To Detail Industry KeywordsGerman AMNOG Process IQWiG Methodology G-BA Procedures#J-*****-Ljbffr

Requirements

Master’s degree or PhD in biostatistics, data science, or a related field Initial experience in HTA, AMNOG, HEOR, or Market Access (industry, consultancy, or research institute preferred) and/or in clinical development Solid understanding of clinical study designs, endpoints, and statistical principles Familiarity 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 advantage Strong analytical skills and attention to detail Fluent German and English, written and spoken (this is an absolute must) Core Competencies Demonstrates expertise in developing German AMNOG dossiers and conducting scientific assessments of clinical trial data, with a strong foundation in biostatistics and data science. Proficient in statistical principles and familiar with industry standards for clinical study data, ensuring high-quality outcomes in health technology assessment. Hard Skills Statistical Analysis Meta-Analysis Clinical Trial Data Assessment Automation Of Analysis Workflows Indirect Treatment Comparisons Soft Skills Strong Analytical Skills Attention To Detail Industry Keywords German AMNOG Process IQWiG Methodology G-BA Procedures #J-*****-Ljbffr

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