Principal Statistical Programmer Noida

OverviewWorking 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 recent program. Position OverviewThis position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only conceptlevel 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 in different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, highquality manner. This individual will be responsible for implementing all reporting and analysis activities for the sponsor clinical trials. ResponsibilitiesGenerate SDTM, ADaM specifications, datasets, reviewers guide and define.xml files for multiple studiesDevelop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a statistician), and complex graphsDeliver highquality statistical programming results, including developing, validating, and maintaining SAS and/or R programs tailored to clinical development program needsParticipate in overseeing CROs' statistical programming deliverables for multiple clinical studies to ensure highquality results and meet prespecified timelinesSupport the preparation of clinical study reports OverviewWorking 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 recent program. Position OverviewThis position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only conceptlevel 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 in different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, highquality manner. This individual will be responsible for implementing all reporting and analysis activities for the sponsor clinical trials. ResponsibilitiesGenerate SDTM, ADaM specifications, datasets, reviewers guide and define.xml files for multiple studiesDevelop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a statistician), and complex graphsDeliver highquality statistical programming results, including developing, validating, and maintaining SAS and/or R programs tailored to clinical development program needsParticipate in overseeing CROs' statistical programming deliverables for multiple clinical studies to ensure highquality results and meet prespecified timelinesSupport the preparation of clinical study reports