SAS Clinical Programmer, Hopewell, NJ
*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 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*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.
SAS Clinical Programmer, Hopewell, NJ
*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 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*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.