I have a very urgent Direct Client requirement for *SAS Programmer *in *Ridgefield, CT. *Please Let Me Know If you have available candidate, please reply with their word resume, location, rate and contact number.
*Please send me your resume at * *[email protected] <[email protected]>Job Title: SAS Programmer Location: Ridgefield, CTDuration: 12 months to 1 Year* *F2F Interview* 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. Thanks *Satya Raj*|Encore Consulting Services, Inc. 116 S Arlington Heights Road, Arlington Heights, IL - 60005 [email protected] <[email protected]> -- You received this message because you are subscribed to the Google Groups "oraapps" 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/oraapps. For more options, visit https://groups.google.com/d/optout.
