Hi,

 

If you have the perfect match for the below requirement, please forward me 
their most updated resumes along with the pay rate and contact information.

 

Please respond to j...@datagrp.com 

 

 

Face to Face is Must

 

 

Position: SAS Programmer, FDA and SPTM Standards

Location: New Jersey

Duration: 12 + Months

 

Must have experience with Statistical Programming

SPTM standards

MUST HAVE STRONG MAPPING

Candidate will be mapping for submission to the FDA

Have worked on the company's mapping projects to map raw data into standard 
data model; · Wrote mapping programs and mapping specifications. 

 

ü      Converted different formats of data (Excel, SPSS, ACCESS, Plain text 
file) to SAS datasets; manipulate and clean up clinical data.  

 

Also exp in the following... 

ü      Generate tables, listings, and graphics of Phase I to IV clinical 
studies for FDA submission.

ü      Production of ad-hoc reports as clinical requests.

ü      Participation ISS and ISE for NDA submission.

ü      Writing of independent QC program to validate SAS code and outputs.

ü      Perform edits check, program validation and documentation.

ü      Preparation of functional specifications that clearly articulate 
programming algorithms, inputs, outputs and assumptions. 

ü      Address data issues and cooperate with data management department to 
resolve issues, created data issues documents. 

 

 

Thanks & Regards,

 

Joel Garner

Technical Recruiter

Data Group, Inc.



Certified Minority Women Owned Business Enterprise (MWBE) & Small Business 
Enterprise (SBE)


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