JOB DESCRIPTION
As a Senior/Principal 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. This role can be performed as fully remote.
Our values We believe in applying scientific rigor to reveal the full promise inherent in data. We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery. We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities. We prize innovation and seek intelligent solutions using leading-edge technology. RESPONSIBILITIES How you will contribute: Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming.Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).Production and QC/validation programming.Generating complex ad-hoc reports utilizing raw data.Applying strong understanding/experience of Efficacy analysis.Creating and reviewing submission documents and eCRTs.Communicating with and/or responding to internal cross-functional teams and clients for project specifications, status, issues or inquiries.Performing lead duties when called upon.Serving as a team player, with a willingness to go the extra distance to get results, meet deadlines, etc.Being adaptable and flexible when priorities change. QUALIFICATIONS To be successful in this position you will have: Bachelor's degree in one of the following fields: Statistics, Computer Science, Mathematics, etc.At least 8 years of SAS programming experience working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent. At least 6 years of related experience with a master's degree or above.Study lead experience, preferably juggling multiple projects simultaneously.Strong SAS data manipulation, analysis and reporting skills.Solid experience implementing the latest CDISC SDTM/ADaM standards.Strong QC/validation skills.Good ad-hoc reporting skills.Proficiency in Efficacy analysis.Familiarity with the drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.Submissions experience utilizing define.xml and other submission documents.Experience supporting Rare diseases and Gastro Intestinal studies would be a plus.Excellent analytical & troubleshooting skills.Ability to provide quality output and deliverables, in adherence with challenging timelines.Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners. Why Cytel?
Cytel is a Global CRO providing ground-breaking biostatistical software and services to large pharma and emerging Biotech clients globally. With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
At Cytel, our focus is to provide you with a comprehensive and competitive total reward package. In addition, our world-class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
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