*Hi,*
*Please reply to ,* *[email protected] <[email protected]>* *Title: SAS Programmer * *Location: Ridgefield, CT* *Duration: One year* *Local: Highly preferred (must be able to attend a f2f interview)* *NO H1b and Need Local candidate because Interview Mode F2F* *- Advanced SAS Certification required * *- Can be verified via the Public Registry of SAS Certified Professionals.* *JD below:* · Develop and maintain datasets as per the CDISC (SDTM and ADaM) standards; Extract data from various databases; · Develop and maintan programs toanalyze the data and procudereports consisting of Tables, Listings and Graphs that are generated from the available databases; · Apply Programming Development Life Cycle (PDLC) principles; · Develop programs using SAS(Statistical Analysis Software) and SQL; · Perform Programming using SAS softwareanalyzing the clinical trial data to produce the outputs for the clinical trial report; · Prepare specifications and process flow diagrams, and develop programming code logic flowcharts; · Write specifications for the analysis datasets and report (Tables, Listings and Graphs) generation; · Prepare reports to assist management in problem analysis, and submit recommendations for solution; · Create primary and validation programs; · Develop, test, debug and deploy the programs in coordination with other line functions as per standard operating procedures (SOPs); · Maintain study documentation; · Document and revise system design procedures, test procedures, and programming standards; · Analyze user/customer needs and software requirements to determine feasibility of design within time and cost constraints; · Create analysis files (datasets), and reports Tables, Listings and Figures; · Consult with customers about software design, maintenance, enhancement and customization; · Store, retrieve, and manipulate data for analysis and reporting; · Expand or modify existing programs for efficiency and reusability; and · Work on other ad hoc tasks as assigned. · Skills: · 1 - 3 years Pharma experience supporting clinical trials Working experience for clinical data; Familiar with trial analysis Familiar with SAS · Education: · Bachelors' Degree or equivalant experience MS Biostat - Advanced SAS Certification required - can be verified via the Public Registry of SAS Certified Professionals. *Vineet Mishra* *Technical Recruiter* 1 Point System LLC Unit 103, 206 N College St, Pineville, North Carolina, 28134 *P*: *803-317-2541* *E* : [email protected] -- You received this message because you are subscribed to the Google Groups "Exact Match" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at https://groups.google.com/group/exact-match. For more options, visit https://groups.google.com/d/optout.
