A new Job, ID: 71994 was added at eJobsVille.com - For the Best Tech Jobs in Town
Title: SAS Clinical Programmer posted on 2013-11-21 14:15:23
Job Description:
Hi Associates,
Hope you are doing great...!!!
Hope you are doing great...!!!
NOTE : IMMEDIATE START !! Only Local to CA..!!!!!
In person interviews will be conducted after phone screen.
Job: SAS Programmer (40772)
Duration- 8+ months Contract
Location: Santa Rosa, CA
Client : Medtronic
*upon offer, candidates must complete background check and drug test*
Duration- 8+ months Contract
Location: Santa Rosa, CA
Client : Medtronic
*upon offer, candidates must complete background check and drug test*
Required
· Industry experience (HealthCare, Pharmaceutical, Medical Device, etc.)
· Development in SAS BASE/STAT/MACRO/SQL
· Industry experience (HealthCare, Pharmaceutical, Medical Device, etc.)
· Development in SAS BASE/STAT/MACRO/SQL
Responsibilities:
Plans and coordinates programming, testing, and documentation of statistical programs for use in creating statistical tables, graphics, and listing summaries.
Programs analysis database manipulations and transfers of data for internal and external clients. May integrate databases from multiple studies or sources.
Develops listing and table specifications with study Biostatistician.
Interact with Data Management and Biostatistics staff and SP team members to negotiate timelines, responsibilities, and deliverables.
Understands and complies with Standard Operating Procedures and Work Instructions.
Programs, tests, and documents statistical programs and tools in accordance with SP standards and validation procedures.
Plans and coordinates programming, testing, and documentation of statistical programs for use in creating statistical tables, graphics, and listing summaries.
Programs analysis database manipulations and transfers of data for internal and external clients. May integrate databases from multiple studies or sources.
Develops listing and table specifications with study Biostatistician.
Interact with Data Management and Biostatistics staff and SP team members to negotiate timelines, responsibilities, and deliverables.
Understands and complies with Standard Operating Procedures and Work Instructions.
Programs, tests, and documents statistical programs and tools in accordance with SP standards and validation procedures.
Requirements:
Experience using SAS for more than 2 years and using SAS on clinical trial data analysis.
Industrial experience is preferred
Regulatory submission experience is a plus
Prefer the candidate has industry experience and had experience with PMA submission etc.
Absolute skill is SAS programming skills inlcuding SAS BASE/STAT/MACRO/SQL etc.
Experience using SAS for more than 2 years and using SAS on clinical trial data analysis.
Industrial experience is preferred
Regulatory submission experience is a plus
Prefer the candidate has industry experience and had experience with PMA submission etc.
Absolute skill is SAS programming skills inlcuding SAS BASE/STAT/MACRO/SQL etc.
Note: We are working with the Preferred Vendor.
Click here to view full job description and apply (Guest users can also apply)
Best regards,
eJobsVille.com - For The Best Tech Jobs In Town
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