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Date:   Wed, 28 Mar 2001 09:55:47 -0500
Reply-To:   Darren Gutowski <darren@GSEARCH.COM>
Sender:   "SAS(r) Discussion" <SAS-L@LISTSERV.UGA.EDU>
From:   Darren Gutowski <darren@GSEARCH.COM>
Subject:   SAS Opportunity in NJ and NY
Content-type:   multipart/alternative;

Global Search is looking for qualified candidates to fill the following positions. If you are a green card holder or U.S. Citizen and have pharmaceutical experience please contact me. Sincerely, Darren Gutowski Global Search Inc. Phone: 973-781-1900x301 Fax: 973-781-1999 8 Wood Hollow Road Parsippany, NJ 07054 Email: darren@gsearch.com http://www.gsearch.com

SAS Programmer -Major Pharmaceutical Corp., Central NJ.

Education: B.S. Computer Science, Statistics or related degree. M.S. degree preferred.

Experience: Proven experience in SAS programming in clinical trials for a minimum of 2 years. Knowledge of a variety of different SAS modules including BASE, STAT, GRAPH, MACRO. Able to work within a team environment with genuine enthusiasm and commitment. Clear and effective communication skills. Ability to write concise and accurate documentation. Understanding of Windows, knowledge of Excel, Word, familiarity with the Clintrial system. Awareness of clinical trial and clinical data management processes. Relevant industry experience in programming for clinical trials including regulatory submissions.

Job Details: Programming support and advice to statistics and data management. Develop, test, validate, implement, document and maintain the departmentıs software library. Produce tables, listing and graphs for clinical study reports. Interact with Regulatory Affairs in support of electronic submissions. Importing and exporting data files. Manipulating and validation of data transfer and transformation programs. Develop and maintain appropriate SOPıs. Identify and implement data management tools in line with the industry. Train users in new applications.

STATISTICAL PROGRAMMER -Major Pharmaceutical Corp., New York, NY Research and Development Description of Duties and Responsibilites: Evaluate Case Report Form (CRF), annotate CRF and SAS data structure Evaluate statistical analysis plan. Perform data validation in SAS. Program tables and listings in SAS. Perform statistical analysis in SAS. Requirements: 2-3 years SAS programming, including statistical procedures and macros. Statistics degree and Pharmaceutical experience a plus. Good communication skills.


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