Responsibilities and Requirements :
- Organize clinical trial data (e.g., integrate EDC datasets to analyze data, generate descriptive summaries, etc.) via R.
- Generate TLFs (emphasis on figures).
- Review and validate SDTM & ADaM datasets has context menu.
- Looking for an R statistical programmer / analyst (with SAS experience as well) to support a small biotech.
- There is not a computing environment set up yet so the person will use the R Studio desktop app and leverage R (like R Shiny) for data visualization.
- This role will require someone who is creative & resourceful in researching and grabbing R packages from the open-sources and at least 3-5 years of clinical trial development experience.
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