*Send the profile to [email protected] * We have a opening, 18 months in duration, for strong SAS clinical programmers.
Client: Non-profit organization Location: NY Rate: $38/hr best (job is secured for 1.5 years) JOB DESCRIPTION: Individuals in this position will work closely with the research teams to generate SAS programs for the analysis and the reporting of data from clinical trials for NDA submission, and for quality control and quality assurance processes. RESPONSIBILITIES: 1. Assist statistical, data management and project teams in the production of statistical reports. 2. Apply statistics/biostatistics knowledge to write and edit statistical programs to evaluate data; produce frequencies, cross tabs, t-tests, life tables and regressions. 3. Participate in edit check program development, testing and implementation as required by in house data management system. 4. Write SAS programs to assist data management team with quality control and quality assurance. 5. Interact with study team members to discuss programming & data issues including synthesis of different data management systems i.e. DataFax and Smart Pen. 6. Participate in the ongoing preparation of SAS datasets for statistical analyses and presentations, e.g. listings, tables and graphics. 7. Participate in the preparation of the final databases for analysis. 8. Integrate and rationalize datasets when necessary. 9. Other data-related requests as assigned REQUIRED SKILLS: 1. B.A./B.S. in computer science, or related field, and a minimum of five years' SAS programming experience, particularly related to pharmaceutical clinical trials; M.S. in computer science statistics/biostatistics or related field desirable 2. Must have extensive knowledge of macro programming, the GRAPH and REPORT procedures. 3. Experience producing displays for FDA submission required. Knowledge, with prior production of displays, related to tabulation and statistical analysis preferred. 4. Experience in helping to design CRFs with statisticians, CRAs and data managers a plus 5. Experience with relational databases & clinical trials required 6. Excellent analytical skills with exceptional attention to detail. 7. Experience with MedDRA and/or WHOART coding for adverse events of clinical trials preferred. 8. Ability to work independently & as part of a team. 9. All candidates must have proof of authorization to work in the U.S. -- Alex Sr.Recruiter [email protected] Atlantis Technologies Inc. 5745 Weddington Dr, Cumming, GA 30040 www.tekatlantis.com -- You received this message because you are subscribed to the Google Groups "ORACLE DWH DBA" 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-dwh-dba?hl=en.
