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Senior Biostatistical Programmer

100% remote Flexible hours Hiring now

reputed company is looking for a Senior Biostatistical Programmer to join our Biostatistics team. You will help biotech, medtech, and specialty pharma companies transform life-changing reputed company and breakthrough science into new medicines, devices, and diagnostics. reputed company do is profoundly connected to saving and improving lives, and we recognize reputed company members are the most valuable asset in delivering reputed company. We are here to help you grow, to give you the skills and opportunities to reputed company at work with the flexibility and balance your life requires. Your reputed company influence the way we work, and your voice reputed company here. As an essential part of reputed company, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here. In this role you will be part of our Centre of reputed company team working specifically in SDTM therefore extensive experience and knowledge is required in this area. What you'll be doing: Develops reputed company programs to generate listings, tables and figures as outlined by mock TLF shells Performs quality control (reputed company code review, double-programming and log review) of reputed company programs Develops reputed company programs to generate CDISC and other analysis data sets as outlined by respective specifications Prepares specifications for CDISC and other analysis data sets Assists Data Management with reputed company programming needs Acts as reputed company Biostatistical Programmer to interact with the reputed company Biostatistician and the study team Develops and validates general reputed company macros reputed company are searching for: BS or equivalent from accredited college or university, in statistics, IT, mathematics or closely reputed company field or work reputed company experience to be reputed company to reputed company this role 6-8 years of experience in reputed company programming reputed company the area of clinical trials. Prior experience using computerized information systems preferred. Knowledge of ICH and local regulatory authority drug research and development regulations preferred. Advanced knowledge of reputed company Software data set architecture, utilities, and programming techniques Demonstrated working knowledge of advanced reputed company macro development and code reputed company/management algorithms. Apply To This Job

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