▷ [High Salary] Principal Statistical Programmer Fsp

Job Category Statistical Programming - FSP 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 Principal 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 Position Overview This position reports to the Director Biostatistics and Programming in the FSP Services business unit in Cytel The Principal Statistical Programmer works independently with only concept level instruction and very little supervision tracks progress and provides expert technical support to team members We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent high-quality manner This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials Responsibilities As a Principal Statistical Programmer your responsibilities will include Generate SDTM ADaM specifications datasets reviewer s guide and define xml files for multiple studies Develop SAS programs which generate datasets complex listings tables including those with descriptive and standard inferential statistics in collaboration with a Statistician and complex graphs Deliver high-quality statistical programming results including developing validating and maintaining SAS and or R programs tailored to clinical development programs needs Participate in overseeing CRO s statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines Support the preparation of clinical study reports regulatory submissions publications annual DSUR and exploratory analyses Understand and follow FDA regulations which affect the reporting of clinical trial data This includes good clinical practice and guidelines for electronic submissions Contribute to the creation maintenance documentation and validation of standards for programming tools outputs and macros Participate in the development of CRFs edit check specifications and data validation plans Provide review and or author data transfer specifications for external vendor data Collaborate with internal and external functions e g CROs software vendors clinical development partners etc to ensure meeting project timelines and goals Provide review and or author SOPs and or Work Instructions related to statistical programming practices Qualifications 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 At a minimum bachelor s degree in computer science data science mathematics or statistics major preferred 7 years of experience as a Statistical Programmer on a Biotech Pharma Clinical Development Biometrics Team or with a similar team and experience supporting drug development medical device development or intervention studies Exceptional SAS programming skills and expertise in the development and implementation of statistical programming procedures and processes in a clinical development environment Extensive applied experience of CDISC standards SDTM ADaM and Define xml medical terminology clinical trial methodologies and FDA ICH regulation Experience supporting regulatory submissions interacting with the FDA and or global regulatory authorities Must be able to work independently Outstanding communication skills written and verbal and strong leadership skills Preferred Qualifications nice to have Prior work experience with pharmacokinetic data and the neuroscience field proficiency in languages or tools other than SAS e g R Python and Java Shiny Markdown Unix Linux and git About Us Cytel is the largest provider of statistical software and advanced analytics for clinical trial design and execution For over thirty years Cytel s scientific rigor and operational excellence have helped biotech and pharmaceutical companies navigate uncertainty prove value and unlock the full potential of their data Come be a part of a team where talent experience and scientific rigor come together to advance the state of clinical development As the industry s largest provider of statistical software and advanced analytics Cytel is home to some of the most innovative collaborative and rigorous biostatistics statistical programming and data management talent Cytel careers offer meaningful work and stimulating challenges within a welcoming and diverse global culture Whether your specialty is biostatistics statistical programming adaptive clinical trial design clinical data management Bayesian statistics real-world evidence artificial intelligence health economics or a corporate function you will be growing an exciting career while contributing to advancing the future of human health at Cytel Search our open jobs or get in touch today to find your fit