*Title: SAS Clinical Programmer* *Location: Hopewell, NJ *
*Duration: 6+ months* *Description:* In this role, you will: - Use your expert knowledge of SAS to integrate clinical data and pharmacokinetic data for pharmacometric analysis. - Create analysis data sets by integrating data from diverse sources for exploration in client TR&D teams. You will participate in this exploration. You will be trained in the use of the Spotfire visualization software, become an expert resource, and lead teams in the use of Spotfire. - Attain subject matter competence in pharmacokinetics, pharmacodynamics, and other scientific areas sufficient to partner with experts to integrate data sources efficiently and effectively. - Meet these goals primarily by programming at an expert level in SAS on UNIX systems, and by creating effective visualizations in Spotfire. - Be trained to competence as necessary in Spotfire, R, Python, and various Linux/UNIX tools including bash and GNU make. - Prepare tables, listings, and figures, and assist in the preparation of pharmacometric reports, for filing with health authorities and responses to queries from health authorities. *Required Skills:* - Excellent skill in the SAS programming language, especially the SAS DATA step and PROCs necessary to manipulate data. - Ability to implement sophisticated algorithms to derive complex data sets and address data issues. - At least two years of industry experience in preparing SAS data sets for analysis. - Very strong attention to quality and detail, and the ability to detect data anomalies. - Excellent interpersonal and communication skills. - Bachelor's degree in engineering, science, computer science, mathematics, or statistics. *Desired but not required (training provided as needed):* - At least two years' experience preparing data sets for pharmacometric analysis in NONMEM, NLME, or WinNonLin. - Master's or higher degree. - Competence in UNIX or Linux, and skill with bash scripting and UNIX filters. - Familiarity with principles of quality control and the validation of computer programs. - Skilled in Spotfire. - Skilled in S+ or R. - Skilled in Python. - Experience with GNU make. - Experience in programming to meet SDTM requirements. - SAS certification in advanced programming or clinical trials. -- Thanks, *Srinadh Reddy* *SILTEK CORPORATION* *people. technology. innovation* 300 Brickstone Square Suite 201 Andover, MA 01810 (978) 475-2500 Direct (978) 623-7201 Fax *sri.sil...@gmail.com <srin...@siltekcorp.com> *www.siltekcorp.com -- You received this message because you are subscribed to the Google Groups "Open Source Erp & Crm" group. To unsubscribe from this group and stop receiving emails from it, send an email to open-source-erp-crm+unsubscr...@googlegroups.com. To post to this group, send email to open-source-erp-crm@googlegroups.com. Visit this group at http://groups.google.com/group/open-source-erp-crm. For more options, visit https://groups.google.com/d/optout.
