176 to 181 of 181 Remote SAS Jobs

current business needs. Technical Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs Author, review, and approve study TFL shells and dataset specifications Author, validate, and document SAS programs for datasets, TFLs, and macros, applying good programming practice Identify data issues and outliers Complete, review, and approve CDISC Validation tool reports Identify data and standards issues and … resolve or escalate as appropriate Maintain proficiency in SAS and awareness of developments Maintain study master file documents and any other documents required to be audit-ready People Management Line management of statisticians, programmers, and other technical staff. Accountable for overall performance of direct reports Provide coaching and mentoring to achieve “excellence”. Direct employee career development and ensure More ❯

current business needs. Technical Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs. Author, review, and approve study TFL shells and dataset specifications. Author, validate, and document SAS programs for datasets, TFLs, and macros, applying good programming practices. Identify data issues and outliers. Complete, review, and approve CDISC Validation tool reports. Identify data and standards issues and … resolve or escalate as appropriate. Maintain awareness of emerging standards and their impact on ongoing and future trials. Maintain proficiency in SAS and stay updated on developments. Maintain study master file documents and other documents required to be audit-ready. People Management Line management of statisticians, programmers, and other technical staff, responsible for overall performance. Provide coaching and mentoring More ❯

current business needs. Technical Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs Author, review, and approve study TFL shells and dataset specifications Author, validate, and document SAS programs for datasets, TFLs, and macros, applying good programming practice Identify data issues and outliers Complete, review, and approve CDISC Validation tool reports Identify data and standards issues and … resolve or escalate as appropriate Maintain proficiency in SAS and awareness of developments Maintain study master file documents and any other documents that are required to be audit-ready People Management Line management of statisticians, programmers, and other technical staff. Accountable for overall performance of direct reports Provide coaching and mentoring of staff to achieve “excellence”. Direct employee More ❯

current business needs. Technical • Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs • Author, review and approve study TFL shells and dataset specifications • Author, validate and document SAS programs for datasets, TFLs and macros, applying good programming practice • Identify data issues and outliers • Complete, review and approve CDISC Validation tool reports • Identify data and standards issues and … resolve or escalate as appropriate • Awareness of emerging standards and associated impact to ongoing and future planned trials • Maintain proficiency in SAS and awareness of developments • Maintain study master file documents and any other documents that are required to be audit ready People Management • Line management of statisticians, programmers and other technical staff. Accountable for overall performance of direct More ❯

package. The role involves providing programming support across various projects and therapeutic areas, with potential supervisory responsibilities. Key Responsibilities Technical tasks include reviewing clinical trial documents, authoring and validating SAS programs, identifying data issues, maintaining audit-ready documentation, and staying updated on standards. People management involves line managing staff, coaching, mentoring, and onboarding. Project management includes overseeing client projects More ❯

providing programming support across various projects, clients, and therapeutic areas, with potential supervisory responsibilities. Key Responsibilities Technical tasks include reviewing clinical trial documents, authoring and reviewing study datasets, validating SAS programs, identifying data issues, maintaining audit-ready documentation, and staying updated on standards. People management involves line managing statisticians and programmers, coaching staff, onboarding new team members, and providing More ❯