-- 

*Dear Associates !*

I am *Ahmed from Sage Group Consulting, Inc*, Please find the job
descriptions below and if you are interested and available for this
position please *send me your updated resume* along with contact number.

*Please send me resume to z <ah...@maccadin.com>ah...@sagetl.com
<ah...@sagetl.com>*



*SAS Programmer - Phase IV*

*6 month + contract*

*Wilmington DE*



I have a new on site 6 month + contract opening with a Pharmaceutical
company in Wilmington DE. They are looking for a SAS programmer to do Phase
IV work, but said that experience wasn’t necessary coming into the project,
so someone who has done more mainstream Phase II and III Trial work would
suffice. Candidates need to be within driving distance for a face to face
interview.



Main responsibilities:

•             Work with statisticians to conduct and/or validate analyses
of clinical/non-clinical data for scientific meeting presentations,
publications and medical information flyers.

•             Support processes for traceability and reproducibility of
publications in a dynamic and multi-task working environment.

•             Provide analytical programming support for external academic
collaborators as needed

•             Build and maintain integrated safety databases (‘data
warehouses’) for monitoring and safety queries

•             Derive and maintain key analysis datasets and corresponding
data specification documents in the standard study environment



Occasionally, the analyst will also engage in:

•             Analyses for internal Quarterly Safety Reviews (QSRs)

•             Conduct additional analyses that may be needed for formulary
submission dossiers and other health economic outcome research tasks.

•             It is anticipated that this newly created position will also
support the Executive Director in introducing and using software for safety
signal detection of internal clinical studies.



Requirements



•             M.S. degree in statistics, MPH, or related field.

•             A minimum of 3 years of experience in the pharmaceutical or
biotechnology industries with knowledge of statistical programming related
to clinical and non-clinical data in the industry

•             Strong SAS programming skills in data step manipulation,
macro language and major statistical procedures

•             In-depth knowledge in the following areas would be considered
a plus:

•             Familiarity with publication process.

•             Experience in accessing and analyzing large databases for
safety signal detection.

•             Knowledge of analyzing high dimensional data (e.g. cluster
analysis, heat maps, factor analysis).

•             Experience in data mining techniques


*Thanks and Regards*



*Zulfiqar Ahmed*

*Sage Group Consulting, Inc*

W:+ 732 767 0010 X 704 | Direct: 732 851 1637 |Email: zah...@sagetl.com

YM: ahmed_maccadin | Gtalk: ahmed.maccadin

LinkedIn: in.linkedin.com/pub/ahmed-zulfiqar/21/950/44b/

Website: www.sageci.com

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