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SAS Programming Sap Data Models Specialist
(Jobs in Nashville, AL)
 
Requirement id 43636
Job title Specialist
Job location in Nashville, AL
Skills required SAS, Pharmaceutical Experience, Biotechnology Industry, Programming Sap Data Models
Open Date 27-Feb-2015
Close Date
Job type Contract
Duration 6 Months
Compensation DOE
Status requirement ---
Job interview type ---
   Email Recruiter: coolsoft
Job Description Specialist: SAS, Pharmaceutical Experience, Biotechnology Industry, Programming Sap Data Models

5+ years of statistical programming in a clinical trial environment (ie, pharmaceutical, biotechnology, and/or contract research organization industries)
* Experience programming and reporting with Base SAS, SAS/Macro, SAS/STAT, SAS Language, SAS/ODS and SAS/Graph
* Create and review/approve annotated CRF to SDTM datasets
* Responsible for the translation of the SAP into programming specifications for analysis data model (ADaM) datasets
* Create and review/approve study specific documents such as validation plans, risk assessments, as appropriate
* Review and approve key study-related documents produced by other functions, such as case report forms, data management plan, and statistical analysis plan
* Responsible for reviewing the SAP and the TFL specifications, and provide feedback to the statisticians
* Responsible for the development, review, validation, and execution of SAS programs to generate standard (SDTM and ADaM) and non-standards (custom study specific) datasets to be included in reports for submission to regulatory agencies, publications, and other communications as defined in specifications documents
* Responsible for the development, review, validation, and execution of SAS programs to generate presentation-ready output (ie, Tables, Figures, and Listings), to be included in reports for submission to regulatory agencies, publications and other communications as defined in Statistical or Report Analysis Plans
* Write and validate study and product-level macros and utilities
* Review of statistical output and clinical study reports
* Program the integration of databases from multiple studies or sources
* Ensures accuracy, quality, and timeliness of all the work that the programming team does on that project. This includes conducting comprehensive review of all datasets and TFLs before final delivery to client. This can be achieved by writing SAS programs to test key variables within the analysis datasets and documentation review of the validation process
* Responsible for accuracy and reliability of results. Builds and monitors quality in every aspect of job activities
* Knowledge of statistical computing applications such as Base SAS, SAS/STAT, and SAS Macro
* Knowledge of relational databases
* Knowledge of statistics and/or clinical drug development process
* Understanding of FDA/ICH guidelines
* Experience with industry data standards, such as CDISC/SDTM, ADaM data models."
 
Call 502-379-4456 Ext 100 for more details. Please provide Requirement id: 43636 while calling.
 
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(Specialist: SAS, Pharmaceutical Experience, Biotechnology Industry, Programming Sap Data Models in Nashville, AL)
     
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