Senior/Principal Statistical Programmer

<strong>Sponsor-dedicated:</strong>   Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. <br/>  <strong>Position Overview: </strong> <br/>  As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM &amp; ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote. <br/>  <strong>Our values</strong> <ul> <li>We believe in applying scientific rigor to reveal the full promise inherent in data.</li> <li>We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.</li> <li>We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.</li> <li>We prize innovation and seek intelligent solutions using leading-edge technology.</li> </ul> <p><strong>How you will contribute:</strong></p> <p> </p> <ul> <li>Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming</li> <li>Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)</li> <li>Production and QC / validation programming</li> <li>Generating complex ad-hoc reports utilizing raw data</li> <li>Applying strong understanding/experience of Efficacy analysis</li> <li>Creating and reviewing submission documents and eCRTs</li> <li>Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries</li> <li>Performing lead duties when called upon</li> <li>Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.</li> <li>Being adaptable and flexible when priorities change</li> </ul> <p> </p> <p><strong>Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have: </strong>   </p> <ul> <li>Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.</li> <li>At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical &amp; Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above.</li> <li>Study lead experience, preferably juggling multiple projects simultaneously preferred.</li> <li>Strong SAS data manipulation, analysis and reporting skills.</li> <li>Solid experience implementing the latest CDISC SDTM / ADaM standards.</li> <li>Strong QC / validation skills.</li> <li>Good ad-hoc reporting skills.  </li> <li>Proficiency in Efficacy analysis.</li> <li>Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.</li> <li>Submissions experience utilizing define.xml and other submission documents.</li> <li>Experience supporting immunology, respiratory or oncology studies would be a plus.</li> <li>Excellent analytical &amp; troubleshooting skills.</li> <li>Ability to provide quality output and deliverables, in adherence with challenging timelines.</li> <li>Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.</li> </ul> <p> </p> <p><span>#LI-KO1</span><br/>#CYTELINT</p>