Clinical SAS/R Programmer - Katalyst Healthcares & Life Sciences
South Plainfield, NJ 07080
About the Job
Responsibilities and Requirements:
- Develop and maintain SAS programs to import, clean, and validate clinical trial data.
- Use R for data manipulation, analysis, and visualization.
Perform statistical analyses in accordance with study protocols and analysis plans. - Generate tables, listings, and figures (TLFs) using SAS and R.
Create and QC statistical outputs and clinical study reports for regulatory submissions. - Document programming activities and ensure compliance with Standard Operating Procedures (SOPs).
- Work closely with biostatisticians, data managers, and clinical researchers.
- Provide programming support for ad-hoc analysis requests and exploratory data analyses.
- Perform rigorous quality checks on all deliverables.
- Minimum of 5years of experience working for large pharma's/CROs .
Source : Katalyst Healthcares & Life Sciences
