*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.* -- You received this message because you are subscribed to the Google Groups "Oracle Users" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at https://groups.google.com/group/oracle-users. For more options, visit https://groups.google.com/d/optout.
