Senior/Principal Statistical Programmer SAS + R (Remote)**Sponsor-dedicated:**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 general 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.**Position Overview:**As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADa M) 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.**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 ADa M 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 e CRTs+ Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries+ Performing lead duties when called upon+ Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.+ Being adaptable and flexible when priorities change**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:**+ Bachelor's degree in one of the following fields Statistics, Computer Science, Mathematics, etc.+ At least 8 years of SAS programming 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 preferred.+ Strong SAS data manipulation, analysis and reporting skills.+ Solid experience implementing the latest CDISC SDTM / ADa M standards.+ Strong QC / validation skills.+ Good ad-hoc reporting skills.+ Proficiency in Efficacy analysis.+ Familiarity with 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 immunology, respiratory or oncology 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.#LI-KO1Cytel Inc. is an Equal Employment / affirmati...#J-18808-Ljbffr

📌 Senior Clinical Rater - Cns Trials Data Integrity (Granada)
🏢 Brooklyn Health
📍 Granada