Key Responsiblities

Strong SAS data manipulation, analysis and reporting skills- with strong output programming experience

Strong proficiency implementing the latest CDISC SDTM / ADaM standards.

Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.

Development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings, figures)

Develop and review SAS programs for data analysis, tables, figures, and listings, and ensure accuracy and consistency of data output

Qualifications:

Bachelor’s or Master’s degree in a data science field, e.g., statistics, mathematics, computer science, bioinformatics,

Minimum 4 years of SAS programming experience supporting clinical trials in the Pharmaceutical & Biotech industry.

Strong expertise in SAS programming, and proficiency in other statistical software such as R and Python

Onsite in Noida , Uttar Pradesh