1. Base SAS and Advance SAS.2. Clinical Research, Clinical Data Management,Pharmacovigilance & SAS Domain Awareness. 3. Robust Knowledge on ICH-GCP Guidelines and GVP Modules.4. Sound Awareness of relevant regulations including 21 CFR part 11. 5. Knowledge on drug development (Phase I-IV) of clinical trial.6. Understands the Study documents (Protocol, eCRF,Dataset specifications, SAP, Mock shells etc.).7. Proficiency in creating SAS data sets, tables, report and graphs, and automatically send to various destinations (including HTML, RTF, PDF, Printer, and Listing) by using SAS ODS statement, as well as convert various file types to SAS Datasets.8. knowledge in CDISC-SDTM Domains like Demographics (DM), Adverse Events(AE).9. Experience in CDISC-ADAM Domains like ADSL,OCCDS and BDS as per current ADaMIG. 10. Demonstrated skills in applying Base SAS, SAS/ MACRO, SAS/ODS, SAS/GRAPH, and SAS/SQL.