Sr Statistical Programmer

As a qualified candidate for the position, you will be responsible for utilizing your strong SAS data manipulation, analysis, and reporting skills, along with a robust output programming experience. Your expertise in implementing the latest CDISC SDTM/ADaM standards will be essential for this role. Additionally, your familiarity with the drug development life cycle and experience in manipulating, analyzing, and reporting clinical trials data will be crucial. Your primary responsibilities will include the development and execution of statistical analysis and reporting deliverables, such as safety and efficacy analysis datasets, tables, listings, and figures. You will also be expected to develop and review SAS programs for data analysis, tables, figures, and listings to ensure the accuracy and consistency of data output. To be considered for this role, you must hold a Bachelors or Masters degree in a data science field, such as statistics, mathematics, computer science, or bioinformatics. A minimum of 4 years of SAS programming experience supporting clinical trials in the Pharmaceutical & Biotech industry is required. You should also possess strong expertise in SAS programming, as well as proficiency in other statistical software such as R and Python. This position is based onsite in Noida, Uttar Pradesh.,