Please do not reply, send your resume on [email protected]
Hi Friends,
Hope your day is going well!
Please send me matching profiles to [email protected] ASAP. Please go through
the requirement thoroughly and submit matching resumes!
Face to Face is Must
SAS PROGRAMMER, FDA AND SPTM STANDARDS12 + MONTHS, NJ
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.
· 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...
· Generate tables, listings, and graphics of Phase I to IV clinical studies for
FDA submission. ·
Production of ad-hoc reports as clinical requests. ·
Participation ISS and ISE for NDA submission. ·
Writing of independent QC program to validate SAS code and outputs. ·
Perform edits check, program validation and documentation.
· Preparation of functional specifications that clearly articulate programming
algorithms, inputs, outputs and assumptions.
· Address data issues and cooperate with data management department to resolve
issues, created data issues documents
Regards,
Bernard D'Souzza
Account Manager - Data Group Inc
Certified Minority Women Owned Business Enterprise (MWBE) & Small Business
Enterprise (SBE)
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Office: 732-791-2348 Ext: 242 | Fax: 732-907-1174 |email: [email protected]|
Website: www.datagroupinc.net|
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