Requirement:-

• Must have experience integrating data sets from archived and current studies
• Must have 8 Years+ Experience in SAS Programming.
• Experience using industry standards for data set design as defined by Clinical Data Interchange Standards Consortium (CDISC)
• Knowledge of appropriate FDA and other regulatory (i.e., ICH) guidances
• Excellent working knowledge of Base SAS, SAS/STAT, SAS Macro language and SAS SQL; SAS/GRAPH a plus.  Experience using SAS version 8.2, 9.1.3 or 9.2
• Provide statistical programming support and validation and help set specifications of analysis datasets, pooled datasets, statistical tables, summaries, figures and listing for Phase II-IV clinical trials. Employ standardized programs where applicable.
• Provide input into planning documents such as protocol, validation plan, and report analysis plan.
• Provide outputs for clinical study reports, integrated summaries and electronic submissions.
• Experience in creation and maintenance of analysis data sets, integration of safety and efficacy data, production/validation of output, and review of annotated case report forms
• Establish and maintain sound working relationship and effective communications within biostatistics and statistical reporting and clinical research. 5+ years of Analytical experience.
• BA/BS or equivalent experience in computer science, mathematics, statistics, life sciences, or related field(s).
• Excellent understanding of clinical trial practices, procedures and methodologies.
• Excellent verbal and written communication skills.
• Good interpersonal and organizational skills. Attention to detail and correctness. Working knowledge of office tools