Hi Partners,
Please find below requirement and kindly send me suitable profiles ASAP Location: North Wales, PA Duration: 6 months SAS-Clinical Trials. MUST HAVE SAMPLE CODE TO SUBMIT A high level of proficiency with SAS's data step, macros, and various procedures is necessary along with excellent verbal and written communications. Familiarity with the clinical trials process is helpful. Relevant programming experience in SAS required. Experience with transforming data in various formats (excel, CSV, ASCII) into SAS datasets is important. Experience cleaning and resolving data issues as well as merging data from different sources into a single integrated dataset is helpful. The incumbent may contribute to documentation. He/she should be prepared to present samples of past work that exhibit consistent, well- structured, mature and high quality SAS programming. He/she is expected to conform to Merck's SOPS and programming practices. Responsibilities: The incumbent will use SAS v9 in a Windows XP environment to support clinical trials. He/she will perform programming and validation to generate analysis datasets and tables for formal clinic Thanks and Regards, *Anil Kumar** * TRUSTEK INC | 1001 Durham Ave, Suite # 101, South Plainfield, NJ 07080 | Work: (908)-462-3134/(732) 393-1313 Ext: 106| Fax: (866)-294-1314| [email protected] | ===================================================================== If you wish not to receive emails any longer - reply with "REMOVE" in subject line ===================================================================== --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "Oracle Users" group. To post to this group, send email to [email protected] To unsubscribe from this group, send email to [email protected] For more options, visit this group at http://groups.google.com/group/Oracle-Users -~----------~----~----~----~------~----~------~--~---
