Senior Statistical Programmer (North America)

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    "description": "<p><span style=\"font-size: 11.0pt\">The Bioforum Biometrics department is growing, and we have an opportunity for an experienced statistical programmer to join our group. This position is in the <span style=\"font-weight: bold\">United States of America (North America)</span>.</span></p>\n<p><span style=\"font-size: 11.0pt\">  </span></p>\n<p><strong><span style=\"font-size: 11.0pt\">Required skills:</span></strong><br></p>\n<ul>\n<li><span style=\"font-size: 11.0pt\">Minimum 6 years’ experience as a statistical programming working on clinical trials.</span></li>\n<li><span style=\"font-size: 11.0pt\">Good knowledge of TFL programming.</span></li>\n<li><span style=\"font-size: 11.0pt\">Experience in programming according to CDISC standards (SDTM, ADaM), and preparing documents for submission (Reviewer’s Guide, Define.xml)</span></li>\n<li><span style=\"font-size: 11.0pt\">Attention to details.</span></li>\n<li><span style=\"font-size: 11.0pt\">Excellent communication skills.</span></li>\n<li><span style=\"font-size: 11.0pt\">A bachelor’s degree in either statistics , computer or life science discipline</span></li>\n</ul>\n<p><span style=\"font-size: 11.0pt\"> </span></p>\n<p><span style=\"font-size: 11.0pt\"> <strong>Duties will include:</strong></span></p>\n<ul>\n<li><span style=\"font-size: 11.0pt\">Participating in all statistical programming activities including preparing clinical data to submission using CDISC or customized standards, reviewing data conversions, data analysis datasets and outputs and taking part in creating best practices and implementation guides.</span></li>\n<li><span style=\"font-size: 11.0pt\">Might need to be responsible for project management (timelines, scope, budget, resourcing) on a project or program level.</span></li>\n<li><span style=\"font-size: 11.0pt\">Train, mentor and share knowledge with the rest of the statistical programming team.</span></li>\n<li><span style=\"font-size: 11.0pt\">Creating programming specification documents for all types of data (SDTM, ADaM, Derived data, etc.).</span></li>\n<li><span style=\"font-size: 11.0pt\">Might include Interaction with customers on a project or program level.</span></li>\n<li><span style=\"font-size: 11.0pt\">Development of SAS programs for conversion of the clinical data based on CDISC or customer instructions.</span></li>\n<li><span style=\"font-size: 11.0pt\">Development of SAS programs for analysis datasets based on SAP, shells and CDISC or customer instructions.</span></li>\n<li><span style=\"font-size: 11.0pt\">Development of SAS programs for study TFLs, based on study SAP and shells.</span></li>\n<li><span style=\"font-size: 11.0pt\">Review and verify all types of conversions and programming done based on customer requirements.</span></li>\n<li><span style=\"font-size: 11.0pt\">Development of core programs for validation, conversion, and maintenance of clinical data dataset structure.</span></li>\n<li><span style=\"font-size: 11.0pt\">Follow the appropriate Standard Operating Procedures (SOPs) for all statistical programming related activities.</span></li>\n</ul>",
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