The position requires a Masters degree in Statistics, Biostatistics, Mathematics, or a related discipline and two 2 years of experience in the job offered, as a Statistical Analyst, Statistical Programming Consultant, or a related occupation.br br The position requires two 2 years of experience with the following Statistical Analysis specifically ANCOVA, Proc Univariate and Proc Mixed procedure of SAS included block, treatments, time and treatment by time interactions in the model; Clinical Trial Analysis with integrated summary of safety ISS and integrated summary of effectiveness ISE analysis; FDA and PMDA submission experience; ADAM datasets creation with ADSL, ADTTE, ADLB with toxicity grading per CTCAE; CDISC including SDTM, ADAM and controlled terminologies; statistical programming processes, and management of statistical programming projects. Must have experience with the following Therapeutic Area; Inflammation, Rheumatology, and Biostatistical Programming Studio BPS; Global Drug Safety Patient Profile creation; and Advanced SAS programming skills and experience in other statistical software, such as R, Python, SQL, GCP and SPlus.
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