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US-NJ: Basking Ridge-Senior Statistical Programmer
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JobCircle.Com  
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 More options Sep 2 2012, 8:30 am
Newsgroups: nj.jobs, alt.bestjobsusa.newjersey.jobs, aol.neighborhood.nj, prg.jobs, comp.jobs
From: newsgro...@jobcircle.com (JobCircle.Com)
Date: Sun, 02 Sep 12 12:30:27 GMT
Local: Sun, Sep 2 2012 8:30 am
Subject: US-NJ: Basking Ridge-Senior Statistical Programmer
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JobCircle.com is the largest regional job board in the
Mid-Atlantic region, with tens of thousands of job offerings
in PA, NJ, DE, MD, NY, and Washington D.C.  To learn more,
visit http://www.jobcircle.com?source=ng
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Job Title:     Senior Statistical Programmer
Job Location:  NJ: Basking Ridge
Pay Rate:      Open
Job Length:    7-12 months (contract)
Start Date:    2012-09-02

Company Name:  Alpha Consulting Corporation
Contact:       attn: Recruiter
Phone:         732-257-3003
Fax:           732-613-9087

Description:   Additional information:                  The manager had mentioned that the candidate needs to know the structure, and understand how data looks.  They will be mainly working on QC work.  There are a lot of Ad Hoc requests and QC datasets needed.                                                                   SENIOR STATISTICAL PROGRAMMER                                                                   REQUIREMENT #12-00157                   RECRUITER:  BRIDGET BURNS                       JOB LOCATION:  BASKING RIDGE, NJ                        JUNE 21, 2012                                                                   PROJECT DESCRIPTION:                    A statistical programmer provides timely support to the study team on all programming matters according to the project strategies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. Should have the ability to generate all of the production tables needed for a given study, and to work with other programmers and statisticians in providing a quality review of the results. Must follow SOPs and department work instructions with a minimum amount of supervision. Has the ability to work on multiple projects and maintain timelines. Knowledge of SAS (Base, Macro, Stats) required, and knowledge of the FDA is desirable, Production programming experience is also a plus.                                 RESPONSIBILITIES:               - Oversees the ad hoc as well as production programming for three to four clinical studies.             - Provides timely support to the study team on all programming matters according to the project strategies.             - Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines               - Implements and executes the programming and project standards.                - Assists in the design and testing of program logic, coding programs, program documentation and preparation of programs.               - Supports ongoing clinical studies requests for statistical and non-statistical analyses. Provides documentation and consistent maintenance of code, logs, and output in a regulated environment.              - Ability to support data cleaning effort, and to work with statisticians and data managers.            - Ability to support study requirements with challenging timelines under direct supervision of the Associate Director of Statistical Programming.               - Support team within a study team involved in the creation and QC of production tables, figures, and listings (TFLs) in support of analysis requirements utilizing Regeneron tools and methodologies.          - Follows department SOPs, and Work instructions as well as Server requirements.                - Supports the marketing activities for the protocols supported.                - Assures that results included in presentation are consistent with results in source /output prior to release.                                                                 EDUCATIONAL REQUIREMENTS:               - Bachelors or Masters degree required          - 2-5 years experience as a Statistical Programmer                              TECHNICAL SKILLS:                       Clinical SAS Programmer responsible for creating tables, listings, figures and analysis data sets.  Consultant should have at least 3 years of clinical SAS experience working in the Biostatistics department.  Good understanding of Analysis Data Sets and Procs.  Experience with STDM, using CDISC, and/or ADaM programming is a plus, but not required. SAS, S-Plus (or R), JMP, and MS Office. Knowledge of FDA requirements is desirable. Ability to work in fast-paced environment is required.                                CORE COMPETENCIES:              - Must be able to work in a consistently busy environment.              - Flexibility and multi-tasking are highly desirable skills for this position.          - Written and oral communication skills                                                                         This 6+ month position starts ASAP.                                             Please E-MAIL your resume (attachment to email) with rate and availability to Bridget: brid...@alphaconsulting.com

Please refer to Job code 12-00157 when responding to this ad.

For FASTEST PROCESSING of your resume, please visit http://www.jobcircle.com/classifieds/11082479.html?source=ng to apply online.

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For fastest processing of your resume, this employer asks that
you apply to this job using the URL above.
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