{"schemaVersion":"jobsearcher.job.v1","id":"95d4e6af378dfcaa71a8ffde","url":"https://jobsearcher.com/jobs/95d4e6af378dfcaa71a8ffde","canonicalUrl":"https://jobsearcher.com/jobs/95d4e6af378dfcaa71a8ffde","title":"Principal Statistical Programmer-FSP","description":"Tech Observer, a Global Clinical Research Organization (CRO) & FSP provider that has been supporting the Pharmaceuticals & Life Sciences Industry since 2005. We have offices in New Jersey, US (Headquarters), India, Denmark, UK & Singapore. Through our local partners, we extend our coverage to Australia, China, Malaysia, South Korea, Taiwan, Thailand, Vietnam, and other countries.\r\nJob Responsibilities ( But not limited to)\r\nCarry out all activities according to Tech Observer/Client SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP). Ensure adherence to programming guidelines.\r\nUnderstanding of Protocol and SAP requirements\r\nLead the assigned project or task\r\nWrite SAS/R programs for development and QC of SDTM datasets, ADaM datasets and reports (i.e. Tables, Listings and Figures)\r\nWrite SAS programs for development and QC of Randomization Schedule\r\nDevelopment and QC of SDTM and ADaM specifications\r\nDevelopment and QC of e-submission package for SDTM and ADaM\r\nReview of study documents such as CRF, Metadata, Protocol, SAP and Mockshells\r\nDemonstrate excellent problem-solving skills, a proactive approach and a willingness to take decisions on a regular basis.\r\nPerform function/project specific responsibilities as assigned\r\nDemonstrate quick learning capabilities to improve programming and domain knowledge\r\nProvide support in the driving system and process improvements, and to develop and implement solutions to improve efficiency and quality of clinical study data processing and reporting\r\nDemonstrate 100% compliance and adherence to all SOPs\r\nPrepare and implement standard operating procedures (SOP)\r\nWrite complex SAS macros\r\nMentor junior statistical programmers and conduct knowledge sharing sessions\r\nWebsite: www.tech-observer.com\r\nLinkedIn: https://www.linkedin.com/company/tech-observer\r\nJ-18808-Ljbffr","company":"Tech Observer","rawCompany":"tech observer","city":"New York","state":"NY","isRemote":false,"isActive":false,"createdAt":"2026-08-08T01:38:18.732Z","occupations":[{"code":"15-2041.00","title":"Statisticians","slug":"statisticians"},{"code":"15-2041.01","title":"Biostatisticians","slug":"biostatisticians"},{"code":"43-9111.00","title":"Statistical Assistants","slug":"statistical-assistants"}],"industries":[{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"},{"code":"541990","title":"All Other Professional, Scientific, and Technical Services","slug":"all-other-professional-scientific-and-technical-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Principal Statistical Programmer-FSP","description":"Tech Observer, a Global Clinical Research Organization (CRO) & FSP provider that has been supporting the Pharmaceuticals & Life Sciences Industry since 2005. We have offices in New Jersey, US (Headquarters), India, Denmark, UK & Singapore. Through our local partners, we extend our coverage to Australia, China, Malaysia, South Korea, Taiwan, Thailand, Vietnam, and other countries.\r\nJob Responsibilities ( But not limited to)\r\nCarry out all activities according to Tech Observer/Client SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP). Ensure adherence to programming guidelines.\r\nUnderstanding of Protocol and SAP requirements\r\nLead the assigned project or task\r\nWrite SAS/R programs for development and QC of SDTM datasets, ADaM datasets and reports (i.e. Tables, Listings and Figures)\r\nWrite SAS programs for development and QC of Randomization Schedule\r\nDevelopment and QC of SDTM and ADaM specifications\r\nDevelopment and QC of e-submission package for SDTM and ADaM\r\nReview of study documents such as CRF, Metadata, Protocol, SAP and Mockshells\r\nDemonstrate excellent problem-solving skills, a proactive approach and a willingness to take decisions on a regular basis.\r\nPerform function/project specific responsibilities as assigned\r\nDemonstrate quick learning capabilities to improve programming and domain knowledge\r\nProvide support in the driving system and process improvements, and to develop and implement solutions to improve efficiency and quality of clinical study data processing and reporting\r\nDemonstrate 100% compliance and adherence to all SOPs\r\nPrepare and implement standard operating procedures (SOP)\r\nWrite complex SAS macros\r\nMentor junior statistical programmers and conduct knowledge sharing sessions\r\nWebsite: www.tech-observer.com\r\nLinkedIn: https://www.linkedin.com/company/tech-observer\r\nJ-18808-Ljbffr","datePosted":"2026-08-08T01:38:18.732Z","dateModified":"2026-08-08T01:38:18.732Z","hiringOrganization":{"@type":"Organization","name":"Tech Observer","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"New York","addressRegion":"NY","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"95d4e6af378dfcaa71a8ffde"},"url":"https://jobsearcher.com/jobs/95d4e6af378dfcaa71a8ffde"}}