Hi Partners,
Please find below requirement and kindly send me suitable profiles ASAP SAS PROGRAMMER, FDA AND SPTM STANDARDS Duration: 12 + MONTHS Location: NJ Must have experience with Statistical Programming SPTM standards MUST HAVE STRONG MAPPING candidate will be mapping for submission to the FDA Have worked on the company's mapping projects to map raw data into standard data model; . - Wrote mapping programs and mapping specifications. - Converted different formats of data (Excel, SPSS, ACCESS, Plain text file) to SAS datasets; manipulate and clean up clinical data. Also exp in the following... - Generate tables, listings, and graphics of Phase I to IV clinical studies for FDA submission. . - Production of ad-hoc reports as clinical requests. . - Participation ISS and ISE for NDA submission. . - Writing of independent QC program to validate SAS code and outputs. . - Perform edits check, program validation and documentation. - Preparation of functional specifications that clearly articulate programming algorithms, inputs, outputs and assumptions. - Address data issues and cooperate with data management department to resolve issues, created data issues documents. - - 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-Distribution" 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-Distribution -~----------~----~----~----~------~----~------~--~---
