Job
- Level
- Lead
- Job Field
- Software, Data
- Employment Type
- Full Time
- Contract Type
- Permanent employment
- Location
- Frankfurt
- Working Model
- Full Remote
Job Summary
In this role, you will develop R packages for clinical trial analysis, build complex R-Shiny applications, and perform statistical programming while leading and training the team on implementations.
Job Technologies
Your role in the 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.
- Leiten Sie die Implementierung in R und schulen Sie andere Mitglieder des Biostatistik-Teams.
- 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).
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Our expectations of you
Qualifications
- 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.
Experience
- 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.
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Benefits
Food & Drink
Health, Fitness & Fun
Work-Life-Integration
Topics that you deal with on the job
Job Locations
This is your employer
IQVIA
Wien
IQVIA is the world's leading provider of data, technology and analytics solutions that help healthcare customers achieve better outcomes. By working with IQVIA, our clients are able to harness today's most advanced technologies and techniques to drive innovation in healthcare - and human health as a whole. As a result, they are making breakthrough progress in areas like business efficiency and patient care.
Description
- Language
- English
- Company Type
- Established Company
- Working Model
- Full Remote, Hybrid, Onsite
- Industry
- Healthcare, Social Sector
R Programming Lead
- Location
- Frankfurt
- Working Model
- Full Remote
- Diversity
- Open for all genders
- English Only
- English only required
