Hi,

We have One Layer between Client and us and if you are Interested to work
with us then Please submit Resumes to sur...@addonusa.com



Statistical Programmers (SAS)

Location: NC

Location: 1 year contract

Rate: $45-50/hr range.



Please send me any qualified candidates you have available that can relocate
to North Carolina for this opportunity.



*Job Description*:



•           Advanced DATA step programming

•           Advanced Functions

•           Advanced Macro

•           Beginner XML

•           Expert ODS

•           Advanced Procedure programming: relevant to clinical trials

•           Advanced knowledge of structured programming principles and
practice

•           Utilize the Validated SAS Programming environment via Citrix
network: Complete training on environment, and utilize macros following
after training and certification.

•           Program, validate, maintain, and document statistical analysis
programs for trials based on SAP and other specified trial documents
following standards and SOPs.

•           Follow specifications (develop specifications if requested) for
SDTM and ADaM datasets, pooled data sets, and TFLs to complete programming
tasks.

•           Ensure that submission and trial data sets (SDTM and ADaM),
TFLs, and other output meet Quality standards.

•           Ensure that data sets, TFLs, and other outputs are produced in
an efficient manner, following standards where applicable.

•           Mentor Associate Statistical Programmers.

•           Advanced SDTM / ADaM Expertise & Experience.

•           Advanced knowledge of CDISC Terminology and Architecture for
both SDTM & ADaM

•           Ability to utilize programming tools to efficiently develop
study specific SDTM and ADaM data sets.

•           Ability to program complex derived trial outcomes for ADaM data
sets

•           Ability to develop and program SDTM Safety Data Pools

•           Intermediate Clinical Trials Design and Analysis Expertise &
Experience.

•           Intermediate understanding of the following:

o          Development Phases

o          Clinical Trials Designs

o          Efficacy Endpoints and Assessments

o          Safety Endpoints and Assessments

•           Intermediate Understanding of ICH E3, E8, and E9 Guidance.

•           Understanding of role of DSMB, CEC, and other trial committees.
Able to provide programming support for these committees as instructed.

•           Advanced ability to identify and prevent programming problems
appropriate to role including:

o          Logic errors and warnings.

o          Inferential statistics programming logic, including appropriate
choice of statistical testing.

o          Appropriate use of trial and program specific macros.

•           Able to leverage software documentation for addressing problems,
and use this knowledge to produce examples for future reference.

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