*Hi,*

*  Good Afternoon.*

*Please send me your suitable consultants regarding the below requirement.*





 *Senior Principle Programmer - SAS - NJ*



• BA/BS degree in life science, statistics, mathematics, computer science,
or related field OR equivalent working experience required.
• 7-10 years Pharmaceutical/CRO experience as a SAS programmer supporting
clinical trials for regulatory submissions.
• Demonstrated knowledge in programming environments, systems and
networking as it relates to the pharmaceutical industry.
• Have in-depth understanding of clinical data structure as well as
relational databases
• Demonstrated proficiency in using SAS
• Demonstrated skills in using software tools and applications, e.g., MS
office, XML, HTML, etc.
• Have an understanding of regulatory requirements pertaining to
technology, systems, and standards.
• Ability to research new technologies and ensure alignment with regulatory
agencies and industry standards
• Demonstrated ability in the handling and processing of upstream data,
e.g., multiple data forms, workflow, eDC, SDTM.
• Demonstrated ability in providing outputs to meet downstream
requirements, e.g., ADaM, Data Definition Table, e-submission


-- 
*Thanks & Regards*
*Raman M*
*REASONSOURCETECH.*

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