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发帖数: 9 | 1 Hi! If any one is interested in the following opportunity of a Senior SAS
programmer in a healthcare company, please submit your resume to the
recruiter:
Stephen Anglin ([email protected]
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The recruiter is a very nice guy!
Job description:
Contract SAS programmer to support data validation in Data Management and
Biostatistics functions. Perform QA activities for the Biostatistics area
in support of the design and interpretation of clinical research/trial data.
RESPONSIBILITIES:
In collaboration with Data Management, programs data review listings,
data integrity checks, and study metrics.
In collaboration with Biostatistics, performs all levels of SAS
programming required by study data validation plans, including parallel
programming of datasets and outputs.
Generates and validates summary tables, data listings and figures for in
-house analyses of study data or publications.
Participates in developing the Statistical Analysis Plan, so that
planned outputs and study endpoint measures are consistent with the study
design.
Develops and maintains SAS macros or other utilities to build quality
into routine SAS programming activities.
Participate in validation of statistical software packages throughout
the software development lifecycle, as needed.
Assist in the validation of work by other programmer/analysts (either
vendor in-house), as needed
REQUIREMENTS:
BS or MS in math, natural science, or information technology
2 or more years’ experience in clinical trials research, either at a
pharmaceutical/biotech sponsor or CRO setting
Proficient in SAS programming with SAS/Base, SAS/Stat and SAS Macro and
SAS/Graph
Knowledge of CDISC theory and implementation guidelines, with an ability
to create and validate SDTM and ADaM datasets with minimal supervision
Excellent attention to detail and problem solving skills |
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