PLEASE SUBMIT ONLY RESUMES, WITH CONTACT INFORMATION, CURRENT LOCATION, AND RATE CONFIRMATION TO AVOID FURTHER DELAY IN SUBMISSION.
Here is the description for the SAS opening I just sent out. Please use this to screen your candidates, anyone who has done mainly Statistical programming for large Pharmaceuticals would NOT be a fit. 6 Month + 50/hr corp to corp is now the top end rate Philadelphia Suburbs SAS Programmer DIS You will be responsible for the annotation of case report forms (CRFs), creation of specifications, programming and validation of data sets and listings, creation and maintenance of supporting documentation and for tasks assigned by DIS management. Responsibilities include, but are not limited to: * Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance. * Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets. * Review CRF annotations produced by other DIS programmers. * Create CRT data set specifications per CDISC or sponsor specified requirements. * Review CRT data set specifications produced by other DIS programmers. * Program CRT data sets per specification. * Validate CRT data sets per the formal, documented QC process. * Create and maintain supporting documentation. * Receive, import, and verify structure of external data. * Program and validate sponsor defined data review listings. * Assist with training and/or mentoring of junior level DIS programmers. * Contribute to departmental process improvements; SOPs and WPs. * Liaise with Data Management and Biostatistics on database specifications, timelines, and quality requirements. * May assist in managing projects as assigned. * May liaise with sponsor as assigned. * Other duties as assigned. * B.S. or local equivalent in computer science, mathematics, life science. * US/CAN/LATAM: A minimum of 3 years of relevant clinical research industry experience, 1 year specifically in the pharmaceutical industry. * EU/AsiaPac: Prior relevant clinical research industry experience, a portion specifically in the pharmaceutical industry. * Working knowledge of CDISC SDTM and CRT-DDS (define.xml). * Experience with statistical programming; analysis data sets, tables, listings, graphs preferred. * Strong organizational, planning and problem solving skills. * Strong oral and written communication skills. * Strong interpersonal skills; team player. Sareen Bhaskaran Resource Manager Prosoft Cyberworld Group 630-371-0530 ext 145 [email protected] YAHOO IM: sareen_prosoftcyberworld PLEASE MARK A CC TO [email protected] --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "Open Source J2EE frameworks" 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/open-source-j2ee-frameworks -~----------~----~----~----~------~----~------~--~---
