CLINICAL SAS PROGRAMMER San Francisco, CA Raritan, NJ SpringHouse, PA 12+ MONTHS Duties: Will develop and validate SAS clinical applications, including Tables, Listings and Graphs (TLG) based upon the SDTM standard. Will develop new, and modify existing macros. May also be developing macros while assuming responsibility for project deliverables. Required: 7+ years’ experience doing SAS Programming for clinical trials Must have NDA submission experience Must be able to work onsite Must possess advanced SAS Programming skills including macro work and ODS Must possess solid documentation skills Must be able to come up to speed quickly in new environment Thanks and Regards, Syeda Afreen Ascentiant International Inc.| Blackhawk Consulting Group| 760 208 4992| afreen@ascentiant.com (primary)| afreen@blackhawkcg.com (secondary)| ____________________________________________ LEGAL NOTICE: Unless expressly stated otherwise, this message is confidential and may be privileged. It is intended for the addressee(s) only. Access to this e-mail by anyone else is unauthorized and may be unlawful. If you are not an addressee, please inform the sender immediately.