Immediate Clinical SAS Role in NJ

[Beth Crowley @ Orbis Data Solutions]

Central NJ
Position Type: Contract

Details: Our client is a midsize pharmaceutical organization that
requires a senior level contract SAS programmer work within their
Inflammation Group.

The Senior SAS programmer will provide statistical programming
technical leadership and support to Data Management. This individual
will participate in the design, development, and quality control
process for SAS programs used to access, extract, transform, review,
analyze, and submit clinical data for phase ll studies. - Codes
complex SAS programs for applications designed to analyze and report
complex clinical trial data and for electronic review, exchange,
transformation, and submission of data in CDlSC SDTM format. The SAS
programmer should have advanced experience with all SAS language,
procedures, and options commonly used in clinical trial reporting
including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH.
Experience with EDC system is required, preferably Inform.

Requirements:
BS in Statistics or Computer Sciences
5-8 years Clinical SAS programming
EDC / Inform


Please contact Beth Crowley at Orbis Data Solutions for more details:

781-569-0607 x1937 or bcro...@orbsidata.com

[Beth Crowley @ Orbis Data Solutions]

Central NJ
Position Type: Contract

Details: Our client is a global pharmaceutical company. They are
looking for a senior SAS programmer for a 6-12 month contract

The SAS programmer will be required to generate the safety and
efficacy tables, listings and graphs required for submissions. They
should have knowledge of CDISC standards as the system will read the
ADaM data sets as input and generate tables, listings and graphs for
the safety summaries for submissions. Custom code may still be
required for efficacy tables, listings and graphs.

Required:
5 years SAS Programming for e- submissions CDISC SDTM ADaM ISS ISE


Please contact Beth Crowley at 781-569-0607 x1937 or email
bcro...@orbisdata.com

Thank you!