Hi,

We have potential openings for the following skills with one of our client.
Please let us know your interest by sending a copy of your resume in MS
Word format.

Full Name:
Current Location:
Contact:
Email: <email%3avangapandu.a...@gmail.com>
Legal Status:
Last 4 digit SSN:
Skype ID for webcam interview:
Availability to start:
Relocation:
Rate:

Couple of References:
Reference:1
Name :
Designation :
Email ID:
Contact :


Reference:2
Name :
Designation :
Email ID:
Contact :

SR Statistical Programmer
Location: Florham Park, NJ
Duration: 12+ Months

*Responsibilities*
·         Writing SAS programs from instructions provided by
Biostatisticians and Statistical Programmers to create CDISC SDTM/ADaM
datasets
·         Generate Define tables and annotated CRFs as per the CDISC and
FDA specifications and guidelines
·         Program in SAS for study report tables/listings/figures, and
submitting the results of clinical trials for investigational medications
·         CDISC SDTM and AdaM models and transforming raw data into these
standards
·         Support data management by generating data listings
·         Conduct QC/Validation of SAS code and output produced by other
Statistical Programmer
·         Work in a team environment providing technical leadership and
solving clinical trial reporting problems of moderate to high complexity
within budget and customary time line constraints while assuring high
quality standards
·         Utilize SAS language, procedures, and options commonly used in
clinical trial reporting including the Macro language, BASE SAS, SAS/STAT
and SAS/GRAPH
·         Create all files, documents, and analyses necessary to support an
electronic submissions in eCTD format, including ISS/ISE

*Qualifications*
·         6+ years of industry experience in SAS programming
·         Excellent programming skill using SAS/STAT, SAS Macro, SAS/SQL,
SAS/GRAPH
·         Good knowledge of 21CFR11 and GCP

-- 
Thanks and Regards,
BenLee
Sr. Recruiter
Vectorsoft
| Email: b...@vectorsoft.com |

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