Law

SAS Statistical Programmer 

Location: Ridgefield, CT

Duration: 12 Months

--Job Description--

 1. Utilizes BI SOPs and guidelines, trial protocols, annotated case report forms, Oracle*Clinical study definitions, trial and project data handling rules and standards, and Statistical Analyses Plans in preparation for the programming of the Data Quality Review Plan (DQRP) and the safety and efficacy tables, listings and graphs (TLG) required for the Clinical Trial Report (CTR) and the associated Analyses Data Sets (ADS).  Gains specific knowledge about the users' environment, data, software and hardware needs

 2. Produce well documented validated standard and non-standard edit check and monitoring programs to support the clinical trial team to ensure the integrity, accuracy and completeness of the data in preparation for clinical reporting.

 3. Review the programming specifications and table mockups in the Trial/Project/Substance Statistical Analyses Plan (T/P/S/SAP) for completeness, correctness and adherence to sited department guidelines and SOPs.  Ensure all programming issues are resolved and updated in the T/P/S/SAP.   Ensure additional specifications once programming commences are properly documented.

 Background:

1-3 years exp supporting clinical trials

 Educational requirements:

MS Statistics/BS Computer Science or Math

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Thanks & Regards..

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