onsite needed : clinical SAS Programmer | Ridgefield, CT

 

clinical SAS Programmer | Ridgefield, CT

LOCAL NEEDED

Duration: 12 Month

Mode of interview: (must be able to attend a 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 maintain programs to analyze the data and procude reports 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 software analyzing 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 equivalent experience MS Biostat

-          Advanced SAS Certification required

-          can be verified via the Public Registry of SAS Certified Professionals.

Garima Gupta | Technical Recruiter | Apetan Consulting LLC

Tel: 201-620-9700* 133 |   mail me  @ garima@apetan.com 

 Ping me  @  garimaapetan133@gmail.com

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