* Strong SAS programming experience with extensive knowledge involving phases (I-III) of clinical trials for MAA (Marketing Authorisation Application), NDS (New Drug Submission) and NDA (New Drug Application) filing.
*Strong experience of CDISC analysis data model (ADaM) and Study Data Tabulation Model (SDTM).
*Extensive Knowledge in producing Tables, Listings and Graphs using SAS.
*Strong knowledge and experience of SAS programming language and experience of using SAS on both Windows and Unix platforms.
*Good working knowledge of ICH, FDA, and GCP regulations and guidelines.