|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|
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.
Global Search Inc.
Phone: 973-781-1900x301 Fax: 973-781-1999
8 Wood Hollow Road Parsippany, NJ 07054
SAS Programmer -Major Pharmaceutical Corp., Central NJ.
Education: B.S. Computer Science, Statistics or related degree. M.S.
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
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.
2-3 years SAS programming, including statistical procedures and macros.
Statistics degree and Pharmaceutical experience a plus. Good communication