Job Details:
 

Information about the position

Job Number:	6106
Job Title:	Senior Statistical Programmer 0901356
Date Posted:	1/1/2010

Job Description:

Description Independently program (or write validation programs for) and document tables/​listings/​graphs for clinical trials or portions of clinical trials requiring routine data manipulation and analysis.​ Routine data manipulation and analysis with limited direction.​ Program (or write validation programs for) and document tables/​listings/​graphs for clinical trials requiring complex data manipulation and analysis.​ Provide input into general standardization efforts and create (or validate) global macros that streamline repetitive operations.​ Mentor biostatisticians and statistical programmer/​analysts with advance SAS programming techniques.​ Interface with SAS technical support to resolve software problems.​ Coordinate, validate and implement SAS upgrades and licenses.​ Independently provide input into CRF specifications to collect data specified in the protocol and query with SAS technical support to resolve software problems, coordinate, validate and implement SAS upgrades and licenses.​ Independently provide input into CRF specifications to collect data specified in the protocol and query check specifications and provide input into analysis plan specifications and data presentations for clinical trials requiring complex data manipulation and analysis.​ Independently program (or write validation programs for) patient randomizations.​ Independently create (or validate) non-standard complex derived datasets.​ Create project and study phase sub-directories ensuring that all project work resides in the correct project and study phase sub-directories.​ Validate study phase flags in oracle tables and download study phase records from oracle tables to create analysis datasets.​ Audit changes to the database between study phases.​ Understand and follow all statistical and statistical programming SOP’s as well as any other relevant SOP.​ Lead process improvement teams as required.​ Effectively communicate analysis specification and programming/​data issues that arise prior to or during analysis in a timely manner.​

Platform:

Required Skills:

Professional Skills & Experience MS, BS (or equivalent).​ 6 years pharmaceutical/​biotech or other relevant experience.​ Fundamental knowledge of relevant statistical areas.​ Fundamental knowledge of relevant clinical areas.​ Advanced knowledge of SAS/​Bas, SAS/​STAT; knowledge of SAS/​Connect, SAS/​Macro, SQL.​ Excellent communication skills Ability to independently solve complex problems logically.​

Desired Skills:

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Information about the company

Company Name:	EMD Serono
Contact Person:	Eric Celidonio
Contact E-Mail Address:
Company Web Site:	https://merckgroup.taleo.net/careersection/2/jobdetail.ftl?lang=en&job=0901356
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Job Poster's Comments:

Please apply online at http://bit.ly/77DNj1