R Programming Lead

Beschreibung

Job Zusammenfassung In dieser Position entwickelst du R-Pakete für die Analyse klinischer Studien, baust komplexe R-Shiny-Anwendungen und führst statistische Programmierung durch, während du das Team bei der Implementierung leitest und schult. Job Zusammenfassung In dieser Position entwickelst du R-Pakete für die Analyse klinischer Studien, baust komplexe R-Shiny-Anwendungen und führst statistische Programmierung durch, während du das Team bei der Implementierung leitest und schult. Deine Rolle im Team Join a sponsor-dedicated team and contribute to the advancement of in-house study activities over time. As the R Programming Lead, you will provide technical expertise to the Statistical Programming team, ensuring the delivery of high-quality solutions that meet both internal and external requirements. Develop internal and external R packages for clinical trial analysis (ADaM, tables, figures, listings). Validate R packages. Building complex R-Shiny applications (animations, dashboards) to address clinical questions, EU JCA requirements, and decision-making. Lead implementation in R and train other Biostatistics team members. Conduct statistical programming work of clinical data using R. Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group. Create and/or validate all safety and efficacy study output requirements (e.g. ADaM, TLFs) consistent with data definitions and specifications and relevant study documentation (e.g. protocol, SAP, aCRF). Collaborates with peers and statisticians to ensure the quality and accuracy -thus submission readiness -of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml). Unsere Erwartungen an dich Qualifikationen Strong programming skills in R/R Shiny. Ability to reproduce statistical analysis using R. Strong skills in data visualization and data wrangling using R. Proficiency in using R packages for data exploration and visualization. Application of statistical methodology and concepts in clinical trial analysis. Advanced knowledge of industry standards including CDISC data structures as well as a solid understanding of the development and use of standard programs. Ability to conduct statistical programming of clinical data using R, and create/validate safety and efficacy outputs (ADaM, TLFs) aligned with study documentation (protocol, SAP, aCRF). Exposure to Late Phase, Real-World Evidence (RWE) & Global Medical Affairs studies is highly desirable. Erfahrung Strong experience in R programming for clinical trial data including developing and validating R packages from CRO or Pharmaceutical Industry. Proven experience in applying R and R-Shiny for the analysis and reporting of clinical trials. Experience with R-Shiny apps for data exploration. Benefits Essen & Trinken 🍏 Frisches Obst Gesundheit, Fitness & Fun 🎳 Team Events 🚲 Jobrad Work-Life-Integration ⏰ Flexible Arbeitszeiten 🏠 Home Office Themen mit denen du dich im Job beschäftigst HealthTech Metadaten Level: Lead Job Feld: Software, Data Anstellung: Vollzeit Vertragsart: Unbefristetes Dienstverhältnis Arbeitsmodell: Full Remote Unternehmenstyp: Etablierte Firma Branche: Gesundheitswesen, Soziales Ort: Frankfurt am Main | Deutschland

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