Urgent requirement for SAS

Hey All

Please find the requirement for Clinical SAS Programmer below. I am looking for Citizen's/GC/H1B who have at least 8 – 9 yrs as SAS Programmer with pharmaceutical clients.   Please be informed that this requirement is thru my prime vendor and there will be a face to face involved here. Looking for consultants who exactly fit the requirement.

JOB SPECS:

SAS PROGRAMMER

BEDMINSTER NJ

6 months Contract

The primary responsibilities includes development and validation of SAS analysis datasets; writing, validating, generating and running customized and standard programs and macros for analyses, tables, listings and graphics from clinical trial data. 

•Identify statistical and programming needs and use standard and customized SAS programs and macros

• Review and modify standard programs appropriately when needed

•Import/export data from/to other data management systems or outside sources,e.g., CROs

•Integrate data from different sources (e.g., SAS datasets from different CROs, CRF data and electronic laboratory data

•Create analysis datasets from raw datasets

 Assess data integrity and validity of data, including edit checks

•Generate statistical analyses and end-of-text tables, figures and listings specified in a statistical analysis plan and in-text tables and figures as specified in the report template

•Create, validate, document, maintain and archive programming specifications and programs

 •Validate standard programs and macros written by other programmers  

•Generate statistical analyses and accompanying tables, figures or listings on an ad hoc basis as requested by other members of the project team after consultation with supervisor.

• Estimate statistical and programming time requirements for team time lines

Establish core corporate standard SAS analysis data set conventions

Establish and maintain corporate SAS MACRO library

Corrdinate with outside vendors to define format specifications for data transfers  

Understanding CDISC stucture for both CRF datasets (SDTM) and analysis datasets (ADAM)

EDUCATION: Master Degree in Statistics, Computer Science, or Life Science or equivalent in experience

 SPECIFIC SKILLS: Three plus years experience of SAS programming in pharmaceutical industry. 

SPECIALIZED SKILLS: Strong SAS skills in SAS BASE, SAS MACRO, SAS STAT languages. Ability to manage timelines and deliverables.     

 

Thanks & Regards,

 

Sue Pandita

Catalyst Systems INC - We Make IT Happen MWBE Certified - Minority Women Business Enterprise

4365 US Highway 1 South, Suite 204

Princeton, NJ 08540

email : sue.pan@catalystsystems.us

609 243 0555 ext 311(work)

732-318-7086 (Cel)

609 243 0557(Fax)

www.catalystsystems.us