Principal/Senior Statistical Programmer (United Kingdom)

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    "description": "<p><span style=\"font-weight: bold\">About the Job</span></p>\n<p>The Bioforum Statistical Programming department is expanding, and we are looking for experienced Statistical Programmers to join our growing team in the United Kingdom.</p>\n<p><br></p>\n<p>If you are passionate about delivering high-quality output for impactful clinical trials, and enjoy leading programming activities in a collaborative environment, this opportunity is for you.</p>\n<p><br></p>\n<p>For this opportunity, <span style=\"font-weight: bold\">oncology trial experience</span> will be a strong advantage.</p>\n<p><br></p>\n<p><span style=\"font-weight: bold\">Required Skills:</span></p>\n<ul>\n<li>B.Sc degree in Life / Computer Science, Statistics, or equivalent.</li>\n<li>Minimum 5 years’ experience working as a Statistical Programmer. Experience leading a team will be an advantage.</li>\n<li>In-depth knowledge of either CDISC SDTM and/or ADaM standards.</li>\n<li>Advanced knowledge of SAS, including SAS Macros.</li>\n<li>Proven ability to program medium- to high complexity statistical output.</li>\n<li>Excellent communication skills.</li>\n<li>Prior oncology experience and/or team leadership experience is advantageous.<br><br></li>\n</ul>\n<p><span style=\"font-weight: bold\">Responsibilities will include:</span></p>\n<ul>\n<li>For Leads: Lead statistical programming teams to deliver on projects and communicate directly with the sponsor.</li>\n<li>Oversee and/or be responsible for the quality and validation of statistical output produced.</li>\n<li>Create or review SDTM and/or ADaM dataset specifications.</li>\n<li>Program and/or validate SDTM and ADaM datasets, and TLFs.</li>\n<li>Provide guidance and input on the statistical programmer requirements and queries during the conduct of the trial.</li>\n</ul>",
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