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Statistical Programmer
| Details |
Country: USA
Location: North Carolina-Raleigh/Durham-RTP RTP, NC 27709
Total applied: 40 |
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Statistical Programmer
SRA International, a dynamic 28 year industry leader whose focus is on providing technology and strategic consulting services to clients in the National Security, Civil Government and Public Health sectors is looking for talented individuals to join our team. Named by FORTUNE Magazine as one of the "100 Best Companies to Work For" 8 years in a row speaks for itself, not to mention our steady financial performance and growth. Our success is attributed to the core values we have stressed since our inception: an ethic of honesty and service; quality work and customer satisfaction; and caring about our people. If you’re looking to make a difference and work on "Missions that Matter" we encourage you to make SRA your employer of choice.SRA International is seeking a Statistical Programmer to join our global drug development business unit. This business unit assists pharmaceutical and biotech clients in all areas of drug development such as: Phase I - IV clinical trials (including clinical monitoring, trials management, data management, statistics and SAS programming); regulatory affairs and product development consulting; quality assurance; medical writing; pharmacovigilence; and programme management. This person will be involved in assisting our current team with both biostatistics for US based clinical trials and also some internationally based clinical trials. Position is full time and based in Durham, NC. 10% travel. Major Responsibilities: Supports the writing of statistical analysis plans and construction of shell tables Reviews documents that have an impact on SAS programming Performs SAS programming for efficacy and safety tables, listings, figures and analyses Performs SAS programming for safety reports Produces tables, listings and figures of data for reports (e.g. Clinical Study Reports, Statistical Reports, etc) Performs QC of tables, listings, figures and analyses Performs SAS program software development and creates associated documentation Provides project manager with regular updates on project progress pertaining to SAS programming activities May solely or jointly coordinate/lead activities/project management for projects within the Data Sciences department May participate in presentations to clients, sites and cross-functional groups Mentors other SAS Programmers Performs other duties as assignedExperience and Skills: Requires Bachelor's degree with a large component of statistics or mathematics Ideally at least 2 years experience in programming in a pharmaceutical company or Contract Research Organization Previous experience in a CRO is preferred Strong working knowledge of SAS Knowledge of Microsoft Word, Excel and PowerPoint High level of proficiency in the full range of essential statistical programming tasks Good analytical ability, excellent attention to detail, and good command of the English language, both written and verbal Understanding of the applicability of ICH GCP to statistics and programming functions Ability to organize, prioritize and multi-task to meet deadlinesTo learn more about SRA International, go to www.sra.com.SRA International is an Equal Opportunity Employer. Company:SRA International, Inc. Reference Code:20014BR
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