Job Brief You will be expected to play a key role in driving the future business road map of the company. We are looking to hire people who are looking to contribute, enhance their skills in latest technology areas and are ready to work in an extremely challenging and fun place to deliver results in very aggressive timeline. Assist in the review of key study-related documents produced by other functions, e.g. SAP, case report form, data management plan, database specifications, EDC data structures, DMC plans and other clinical documents Write, test and validate SAS programs to produce analysis datasets, TLGs and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications Write CDSIC standard dataset specifications and follow specifications to create SDTM and ADaM datasets Understand and execute department-, product- and study-level macros and utilities. Write, test and validate product- and study-level macros and utilities Job ID: CJ0001 Qualifications: Pharma/MS Biostatics/M.tech/Any Pharma Qualification/ Statistical Skills Required: Oncology/SDTM/ADAM/SAS/SAS Macros/Drug Development/Oncology Endpoints/SAS STAT/SAS GTL/ Statistical Methodologies Experience: 7 – 20 Years Job Type: Full Time Salary: As per the Industry Best Responsibilities Assist in the review of key study-related documents produced by other functions, e.g. SAP, case report form, data management plan, database specifications, EDC data structures, DMC plans and other clinical documents Write, test and validate SAS programs to produce analysis datasets, TLGs and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications Write CDSIC standard dataset specifications and follow specifications to create SDTM and ADaM datasets Understand and execute department-, product- and study-level macros and utilities. Write, test and validate product- and study-level macros and utilities.