Senior Statistical Programmer

<strong>Sponsor-dedicated: </strong> <br/>  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 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 Statistical Programmer, you will leverage your advanced SAS programming skills to support or lead one or more Phase I-IV clinical trials.   <p><strong>As a Statistical Programmer, your responsibilities will include:</strong></p> <p> </p> <ul> <li>Performing data manipulation, analysis, and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming</li> <li>Applying your SAS programming skills, to create and validate datasets/analysis files, tables, listings, and figures ( TLF s)</li> <li>Generating complex ad-hoc reports</li> <li>Preparing and validating submission packages</li> <li>Applying your strong understanding/experience with Efficacy analysis</li> <li>Preparing submission packages</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><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>At least 3+ years of relevant experience in statistical programming in the clinical development environment</li> <li>BA/BSc or higher degree in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject</li> <li>Excellent SAS data manipulation, analysis and reporting skills</li> <li>Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data</li> <li>Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners</li> <li>Excellent oral and written English communication skills</li> <li>Ability to provide quality output and deliverables, in adherence with challenging timelines</li> <li>Willingness and ability to learn and follow Company’s standard processes and procedures.</li> <li>Ability to effectively perform complex statistical programming and related tasks</li> <li>Willingness and ability to provide guidance to team members on technical and process questions</li> </ul> <br/>  <strong>Preferred Qualifications:</strong> <ul> <li>In-depth knowledge of SAS Graph and other SAS Statistical packages</li> <li>Prior publication work experience</li> </ul> <p> </p> <p>#LI-KO1<br/>#CYTELINT</p>