Job Description
Role responsibilities:
• Developing R function to generate SDTM, ADaM datasets.
• Developing R function to generate tables, figures, and listings for standard safety reports.
• Developing Rshiny App for dynamic safety review.
Qualifications:
• Bachelor or Master’s degree in a related discipline.
• 1+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
• Strong hands-on experience with R (e.g., Tidyverse, ggplot2, admiral, gt, reactable, etc.)
• Strong Knowledge of Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL and SAS/ODS
• Solid understanding & implementation of CDISC requirement for regulatory submissions.
• Experience working with cross-functional teams.
• Effective communicator.