Details:

Summary of Job Responsibilities: 

 •    Working under the direction of Senior Statistical Programmer/Team Lead, the statistical programmer conducts programming activities for a trial, early phase project, indication, or publication activities. 

•    Read and understand the program specifications document. 

•    Prepare SAS® analysis datasets, tables, listings, and figures as per specifications. 

•    Create programs to create graphs and tables that are required in CSRs, safety reports, efficacy reports, etc. ensuring on-time quality delivery. 

•    Validate and transform data sets as per client assignment specifications. 

•    Validate tables, listings, and figures as per client assignment specifications. 

•    Ability to work on data migration from legacy datasets to standards such as CDISC or any other client specific standard. 

•    Co-ordinate with the client and US-team for clarity of specifications, data issues, outliers, reviews, schedules, etc. 

•    Perform all the above tasks using standard operating procedures (SOPs) as defined in Quality Management System or the respective client(s) as applicable. 

Qualifications and Experience Education: 

Bachelor’s or Master’s degree in Computer Science, Statistics or related Health Sciences field Experience: 

 •    A minimum of 2–3 years of SAS® programming experience with clinical trial data. 

•    General knowledge of regulatory requirements and drug development process. 

•    Fair knowledge of Clinical trial domain and good SAS®programming skills. 

•    Ability to work independently.

Min. Qualification:

ug

Skills Required:

sas, statistics