Cytel - Senior Statistical Programmer

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