Job Title

 Statistical Programmer

Post Date

  

 08 13 2008

Firm

 Major Pharmaceutical Company

Duration

 

 Permanent and Contract

Location

 Central New Jersey, USA

Years Exper.

 

 3 yrs

Industry1

 Pharmaceutical

Salary 

 

  

Industry2

 

 

 

 

Job Description

Job Title: Statistical Programmer 

SAS Duties:  Provide statistical programming expertise (preferably in SAS) in the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of statistical analysis plans. Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical, statistical reports and other similar reports. Contribute to the integrated clinical/statistical report and other similar documents. Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting. Perform quality assurance procedures on work performed by others. Develop, test, validate, document, maintain and execute software and/or systems using the currently endorsed tools or support of production activities. Assist in the integration of data from remote entry sites, contract research organizations and co-licensing partners to the central database.

Skills:  Selected candidate must have at least 3 years of SAS programming experience and at least 1 full year of formal working experience in statistical programming supporting clinical trials; possess high level of expertise in SAS/BASE, SAS/STAT SAS/GRAPH, SAS/SQL, MACRO, ODS, SAS REPORT and SAS/CONNECT areas; and be proficient in data manipulations, report/graph generations using data steps with varies SAS functions, procedures, macros, and ODS facilities; must be experienced with production of data listings, summary tables and graphs for completion of Clinical Study Report and have good understanding of statistical methodologies and clinical trial operations. NDA experience and/or knowledge of FDA regulations are very helpful. Excellent communication skill and teamwork spirit are required.

   

 

Qualifications

 Education:

BS/MS in statistics, mathematics, or computer science. MS in statistics is preferred. SAS Institute certification is highly desirable

   

 

Organization

Aequor Technologies, Inc. is a global IT Consulting & Solutions company that has been providing high value added business solutions to enterprises of all sizes. Headquartered in the United States and with offices across North America as well as high tech global remote development centers in the US and India. Aequor Technologies, Inc. has proven competencies in business and technology.

 

 

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Job Code

  

 URL

  www.aequor.com

Contact  Email

 

basil@aequor.com

Contact Firm 

 Aequor Technologies

Contact Name

 Basil Licop

 

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