Join to apply for the Senior Clinical Data Scientist role at Nanosep AB .
Responsibilities:
- Develop internal and external R packages for clinical trial analysis (ADaM, tables, figures, listings).
- Validate R packages.
- Lead implementation in R and train other Biostatistics team members.
- Create and validate safety and efficacy study outputs (e.g., ADaM, TLFs) in accordance with data definitions, specifications, and study documentation (protocol, SAP, aCRF).
- Conduct statistical programming of clinical data using R.
- Identify problems and develop tools to improve efficiency of the Statistical Programming group.
- Collaborate with peers and statisticians to ensure quality and accuracy of clinical data submissions (e.g., SDTM, ADaM, tables, figures, listings, define.xml).
Qualifications:
- Minimum 5+ years of experience in R programming for clinical trials, including developing and validating R packages from CRO or pharmaceutical industry.
- Strong programming skills in R/R Shiny.
- Understanding of end-to-end clinical trial processes is mandatory.
- Experience with late-phase and RWE studies is desirable.
- Proven ability to apply R and R-Shiny for analysis and reporting, with skills in data visualization and wrangling.
- Knowledge of industry standards like CDISC data structures.
- Deep understanding of clinical trial phases and drug development process.
IQVIA is a leading provider of clinical research services and healthcare insights. Learn more at .
We value diverse talent committed to innovation and impact. Join us to help improve patient outcomes worldwide.
Seniority level
- Mid-Senior level
Employment type
- Full-time
Job function
- Research, Analyst, and Information Technology
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Contact Detail:
Nanosep AB Recruiting Team