Clinical SAS Programmer

Location - Whitelfield JD for Clinical SAS programmer For Sr. SAS Programmer experience level (5 - 8 years) For Pr. SAS programmer experience level (9 – 13 year) Skills Required: Experience of extracting, manipulating, merging, summarizing, analysing, and presenting data using SAS procedures Experience in SDTM and ADAM spec writing and programming is a must Experience in TLF's Strong experience of base SAS programming, Proc SQL, macro programming, ODS and various SAS modules: SAS/GRAPH, SAS/STAT and other modules like SAS/Connect and SAS/Access is a must. Experience with reporting environments and reporting tools related to SAS programming in pharmaceutical industry; proc report, proc summary and proc tabulate. Strong experience in SAS programming in various phases of clinical trial. Experience in pooled data analysis and programming. Strong experience in efficacy reporting with regards to development of analysis sets and treating missing values. Experience in working with relational databases and performance tuning of SAS programming Experience with writing batch scripts and/or shell scripts is a plus Roles & Responsibilities: Responsible for developing and maintaining programming and validation specifications for TLGs as per requirements provided by the Bio statistician Create and maintain SAS programs to produce outputs to support the analysis and reporting of clinical trials Develop analysis datasets for trial level reporting and integrated safety and efficacy activities Program and QC data listings, summaries and Graphs as defined in SAP. If required, validate the statistical models used for programming Develop re-usable utility macros in order to build a macro library to support programming tables, listing and graphs for phase 1-4 clinical trial reporting Collaborate with the project team to ensure the deliverable are completed on time with high quality Create submission-ready standard data presentations and data sets using standard coding and following standard industry processes including SDLC Maintain all project documentation as required by SOP and Processes Mentor statistical programmers Ensure compliance with eClinical Solutions and industry quality standards, guidelines, and procedures Other duties as assigned