*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 oracle-users+unsubscr...@googlegroups.com. To post to this group, send email to oracle-users@googlegroups.com. Visit this group at https://groups.google.com/group/oracle-users. For more options, visit https://groups.google.com/d/optout.