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*Hi,*



Hope you are doing well.



While searching for few profiles on *SAS Programmer*, I came across your
profile on one of the job board and found to be a match. Please mail me your
interest, availability, salary along with the updated resume.


**

Here am forwarding the job description for your
review.

* *

*Job Title: SAS Programmer*

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*Job Location: Paramus, NJ*

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*Duration: 6+ Months*

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*Job Description:*

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   - Coordinate, program, analyze and evaluate clinical data
   - Analyze, write, test, run and maintain programs to generate databases,
   SAS datasets, ASCII files, etc., to be transferred to the FDA as required
   - Analyze, write, test, run and maintain computer programs for reporting
   of data from external sources (i.e., central labs, coding dictionaries,
   etc.)  into the clinical database system
   - Prepare data listing, tables and graphical displays of data in the
   database as required to support data reviews, statistical analysis and
   report writing efforts on a specific project or projects
   - Maintain appropriate documentation files of all programs used to
   process data for a project
   - Prepare data listing, tables and summaries of data in the clinical
   database to support adverse experience regulatory reporting
   - Review CRF's and ensure their design meets the protocol criteria and
   contains all data required to support a high quality database and the
   planned analysis
   - Develop programming specifications for derived data sets, listing
   tables and summary tables in collaboration with study Statistician
   - Create test data and create derived data sets
   - Develop and participate in programming development and validation of
   programming needs for the above
   - Participate in data review and provide feedback on data quality
   - Maintain appropriate study documentation files, data set, program and
   output log files
   - Perform other non-statistical ad hoc requests, patient profiles,
   quality assurance edit checks
   - Review data for adherence to protocol, consistency in handling and
   coding, completeness, accuracy and relevance of final data sets
   - Ensure proper study closeout by documenting and archiving computer
   software and data sets and electronic transfers of the same as required
   - Design, test and implement clinical data validation and derivation
   procedures in the Clinical Data management system and perform on-line review
   of automated validation/consistency checks
   - Enforce Clinical Data integrity i.e., documenting errors, omissions and
   inconsistencies found during clinical database validation process
   - Participate in training of programming and Data Management personnel
   and may lead and direct the work of other programmers as required

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   - Bachelor's Degree with 10 years SAS programming experience, 6 years of
   which represents experience in clinical trials data processing, with
   experience in Proc SQL and Oracle Clinical data extracts or an equivalent
   combination of training and experience


   - Knowledge of relational databases and PL/SQL and familiarity with
   Windows/Windows NT network environment desirable

* *

* *

Thanks & Regards



*Lokesh Muttineni**
SITI Corporation
*408 654 6586
[EMAIL PROTECTED]
www.siti.com



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