Looking for Excellent SAS Clinical with 7-9yrs exp. Location NC Durham


The Senior Programmer provides technical expertise for the conduct of
clinical trials, might act as an internal subject matter expert in specific
areas providing technical support and expert advice, and works independently
to support various programming activities related to clinical systems,
and/or analysis and reporting, and/or the applications/systems within
eClinical technologies. In addition, the Senior Programmer can fill the
Global Technical Services Coordinator role on projects, and liaise with
sponsors, GTS Leads, and other functional areas as required.



-Coordinate project start-up activities, including Unix/PMED project area
set-up, creation of global programs (e.g., setup.sas, formats.sas, etc.),
tracking spreadsheets, and required documentation.

-Assist in the production and QC of analysis plans, TLF mock-shell
development, derived dataset specifications, programming specifications, and
other process supporting documents.

-Use efficient programming techniques to produce and/or QC derived datasets
tables, figures and data listings.

-Understand regulatory requirements concerning industry technical standards
(e.g., CDISC, 21 CFR Part 11, electronic submissions, etc.) and implications
for the department.

-Provide input into monthly PERFORM forecasts and monitor the completion of
forecasted units.

-Create standard macros and applications to improve the efficiency of the
department.



Language Skills

-Excellent English written and oral communication skills.



Minimum Work Experience

-Relevant Clinical Trial industry experience

-Experience working with systems used within the Clinical Trial process
(e.g., SAS, CDMS, EDC (Inform, RAVE, DataLabs), CTMS, Medical Safety
Reporting)







Regards,


[email protected]

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