151 to 175 of 181 Remote SAS Jobs

may vary based on business needs. Technical Review clinical trial documents (protocols, SAPs, CRFs, CSRs) Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices Identify data issues and outliers Review and approve CDISC Validation reports Address data and standards issues appropriately Stay informed … of emerging standards and their impact Maintain proficiency in SAS and stay updated on developments Ensure audit readiness of study documentation People Management Manage statisticians, programmers, and technical staff, overseeing their performance Mentor and coach staff to achieve excellence Handle onboarding and integration of new team members Provide technical leadership and coaching Project Management Oversee key client projects and More ❯

project management. Key Responsibilities Technical Review clinical trial documents such as protocols, SAPs, CRFs, and CSRs Author, review, and approve study TFL shells and dataset specifications Develop and validate SAS programs, ensuring good programming practices Identify data issues and outliers Review CDISC validation reports Resolve data and standards issues or escalate as needed Stay informed about emerging standards and … their impact on trials Maintain SAS proficiency and stay updated on developments Maintain study documentation for audits People Management Manage statisticians, programmers, and technical staff, overseeing performance Coach and mentor staff for excellence and career development Recruit, onboard, and integrate new team members Provide technical leadership and coaching Project Management Oversee key client projects and portfolios Serve as Veramed More ❯

or project management. Key Responsibilities Technical Review clinical trial documents including protocols, SAPs, CRFs, CSRs Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros following good programming practices Identify data issues and outliers Review CDISC Validation reports Resolve or escalate data and standards issues Stay updated on … emerging standards and their impact on trials Maintain proficiency in SAS and monitor developments Keep study master files and audit-ready documents People Management Manage statisticians, programmers, and technical staff, ensuring performance Coach and mentor staff for excellence and career development Recruit, onboard, and integrate new team members Provide technical leadership and coaching Project Management Oversee client projects and More ❯

may vary based on business needs. Technical Review clinical trial documents (protocols, SAPs, CRFs, CSRs) Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros following good programming practices Identify data issues and outliers Complete, review, and approve CDISC Validation reports Address data and standards issues appropriately Stay … updated on emerging standards and their impact on trials Maintain proficiency in SAS and stay informed about developments Ensure study documentation is audit-ready People Management Manage statisticians, programmers, and technical staff, overseeing performance Coach and mentor staff for excellence Handle onboarding and training of new staff Provide technical leadership and coaching Project Management Oversee client projects and portfolios More ❯

on business needs. Technical Review clinical trial documents such as protocols, SAPs, CRFs, and CSRs Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros following good programming practices Identify data issues and outliers Complete, review, and approve CDISC Validation reports Address data and standards issues appropriately Stay … informed about emerging standards and their impact on trials Maintain proficiency in SAS and stay updated on developments Ensure study master files and other audit-ready documents are maintained People Management Manage statisticians, programmers, and technical staff, overseeing their performance Coach and mentor staff to achieve excellence Handle recruitment, onboarding, and training of new staff Provide technical leadership and More ❯

may vary based on business needs. Technical Review clinical trial documents (protocols, SAPs, CRFs, CSRs) Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros Identify data issues and outliers Review CDISC Validation tool reports Resolve data and standards issues or escalate as needed Stay informed on emerging … standards and their impact Maintain proficiency in SAS and stay updated on developments Ensure audit readiness of study master files and related documents People Management Manage statisticians, programmers, and technical staff, overseeing performance Coach and mentor staff to achieve excellence Handle hiring, onboarding, and training of new staff Provide technical leadership and coaching Project Management Oversee client projects and More ❯

on business needs: Technical Review clinical trial documents such as protocols, SAPs, CRFs, and CSRs Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros, adhering to good programming practices Identify data issues and outliers Review and approve CDISC Validation reports Address data and standards issues appropriately Stay … updated on emerging standards and their impact on trials Maintain proficiency in SAS and stay informed about developments Ensure study documentation is audit-ready People Management Line management of statisticians, programmers, and technical staff Coach and mentor staff to achieve excellence Oversee employee career development and training Recruit and onboard new staff effectively Provide technical leadership and coaching Project 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 proficiency in SAS and awareness of developments Maintain study master file documents and other audit-ready documents People Management Line management of statisticians, programmers, and other technical staff, accountable for overall performance Provide coaching, mentoring, and career development for staff Interview, onboard, and integrate new staff members Provide programming technical leadership and coaching More ❯

on business needs. Technical Review of clinical trial documents such as protocols, SAPs, CRFs, CSRs Authoring, reviewing, and approving study TFL shells and dataset specifications Authoring, validating, and documenting SAS programs for datasets, TFLs, and macros, following good programming practices Identifying data issues and outliers Completing, reviewing, and approving CDISC Validation reports Resolving data and standards issues or escalating … as needed Staying aware of emerging standards and their impact on trials Maintaining proficiency in SAS and staying updated on developments Keeping study master files and audit-ready documents People Management Line management of statisticians, programmers, and technical staff, ensuring performance Providing coaching, mentoring, and career development Onboarding new staff effectively Providing technical leadership and coaching Project Management Overseeing More ❯

may vary based on business needs. Technical Review clinical trial documents (protocols, SAPs, CRFs, CRSs) Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices Identify data issues and outliers Complete, review, and approve CDISC Validation reports Resolve or escalate data and standards issues … Stay updated on emerging standards and their impact Maintain SAS proficiency and awareness of developments Keep study master files and audit-ready documents People Management Line management of statisticians, programmers, and technical staff Coach and mentor staff for excellence Manage employee career development and training Onboard new staff members Provide technical leadership and coaching Project Management Oversee key client More ❯

current business needs. Technical Review clinical trial documents such as protocols, SAPs, CRFs, and CSRs Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices Identify data issues and outliers Review and approve CDISC Validation reports Resolve data and standards issues or escalate as … needed Stay informed about emerging standards and their impact on trials Maintain proficiency in SAS and stay updated on developments Maintain study master files and audit-ready documentation People Management Line management of statisticians, programmers, and technical staff, ensuring performance standards Coach and mentor staff to achieve excellence Oversee staff onboarding and training Provide technical leadership and coaching Project More ❯

may vary based on business needs. Technical Review clinical trial documents (protocols, SAPs, CRFs, CSRs) Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros following good programming practices Identify data issues and outliers Review and approve CDISC validation reports Address data and standards issues appropriately Stay informed … about emerging standards and their impact on trials Maintain proficiency in SAS and stay updated on developments Keep study master files and other audit-ready documents People Management Manage statisticians, programmers, and technical staff, ensuring performance Coach and mentor staff for excellence Oversee staff onboarding and training Provide technical leadership and coaching Project Management Manage client projects and portfolios More ❯

may vary based on business needs. Technical Review clinical trial documents (protocols, SAPs, CRFs, CSRs) Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices Identify data issues and outliers Complete, review, and approve CDISC Validation reports Resolve or escalate data and standards issues … Stay informed on emerging standards and their impact on trials Maintain proficiency in SAS and stay updated with developments Maintain study master files and audit-ready documents People Management Line management of statisticians, programmers, and technical staff Provide coaching, mentoring, and career development for staff Recruit, onboard, and integrate new team members Offer technical leadership and coaching Project Management More ❯

vary based on business needs. Technical Review 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, following good programming practices Identify data issues and outliers Complete, review, and approve CDISC Validation reports Resolve or escalate data and standards issues … as appropriate Stay informed about emerging standards and their impact on trials Maintain proficiency in SAS and stay updated on developments Maintain study master file documents to be audit-ready People Management Line management of statisticians, programmers, and technical staff, ensuring performance standards Coach and mentor staff for excellence and career development Onboard and integrate new team members effectively More ❯

on business needs. Technical Review clinical trial documents such as protocols, SAPs, CRFs, and CSRs Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices Identify data issues and outliers Complete, review, and approve CDISC Validation reports Resolve or escalate data and standards issues … as appropriate Stay updated on emerging standards and their impact on trials Maintain proficiency in SAS and stay informed about developments Ensure study documents are audit-ready People Management Manage statisticians, programmers, and technical staff, overseeing their performance Coach and mentor staff to achieve excellence Handle onboarding and training of new staff Provide technical leadership and coaching Project Management More ❯

based on business needs: Technical Review clinical trial documents including protocols, SAPs, CRFs, and CSRs Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros, adhering to good programming practices Identify data issues and outliers Complete, review, and approve CDISC Validation reports Resolve data and standards issues or … escalate as needed Stay informed about emerging standards and their impact on trials Maintain proficiency in SAS and stay updated on developments Ensure study documentation is audit-ready People Management Manage statisticians, programmers, and technical staff, overseeing their performance Coach and mentor staff to achieve excellence Handle onboarding and integration of new team members Provide technical leadership and coaching More ❯

and project management. Key Responsibilities Technical Review clinical trial documents including protocols, SAPs, CRFs, CSRs Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices Identify data issues and outliers Review and approve CDISC Validation reports Address data and standards issues and escalate as … needed Stay updated on emerging standards and their impact on trials Maintain proficiency in SAS and stay informed of developments Ensure audit readiness of study master files and related documents People Management Manage statisticians, programmers, and technical staff, overseeing performance Coach and mentor staff to achieve excellence Handle recruitment, onboarding, and training of new staff Provide technical leadership and More ❯

on business needs. Technical Review of clinical trial documents including protocols, SAPs, CRFs, and CSRs. Author, review, and approve study TFL shells and dataset specifications. Author, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices. Identify data issues and outliers. Complete, review, and approve CDISC Validation reports. Identify and resolve or escalate data and … standards issues. Maintain awareness of emerging standards and their impact on trials. Maintain proficiency in SAS and stay updated on developments. Maintain study master file documents for audit readiness. People Management Line management of statisticians, programmers, and technical staff. Provide coaching, mentoring, and career development for team members. Interview, onboard, and integrate new staff. Provide technical leadership and coaching. More ❯

based on business needs. Technical Review clinical trial documents including protocols, SAPs, CRFs, and CSRs. Author, review, and approve study TFL shells and dataset specifications. Develop, validate, and document SAS programs, ensuring good programming practices. Identify data issues and outliers. Review and approve CDISC Validation reports. Resolve or escalate data and standards issues. Stay updated on emerging standards and … their impact. Maintain proficiency in SAS and stay aware of developments. Keep study master files and audit-ready documents. People Management Line management of statisticians, programmers, and technical staff. Coach and mentor staff, support career development, and ensure training. Interview, onboard, and integrate new staff. Provide technical leadership and coaching. Project Management Oversee client projects and portfolios, acting as 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 audit-ready documents People Management Line management of statisticians, programmers, and other technical staff, responsible for overall performance Provide coaching, mentoring, and career development for More ❯

vary based on business needs. Technical Review clinical trial documents including protocols, SAPs, CRFs, CSRs Author, review, and approve study TFL shells and dataset specifications Develop, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices Identify data issues and outliers Complete, review, and approve CDISC Validation reports Address data and standards issues appropriately Stay … informed of emerging standards and their impact on trials Maintain proficiency in SAS and stay updated on developments Ensure audit readiness of study master files and related documents People Management Manage statisticians, programmers, and technical staff, overseeing their performance Provide coaching, mentoring, and career development for team members Recruit, onboard, and integrate new staff Offer technical leadership and coaching More ❯

on business needs. Technical Review clinical trial documents such as protocols, SAPs, CRFs, and CSRs. Author, review, and approve study TFL shells and dataset specifications. Develop, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices. Identify data issues and outliers. Complete, review, and approve CDISC Validation reports. Address data and standards issues appropriately. Stay … informed about emerging standards and their impact on trials. Maintain proficiency in SAS and stay updated on developments. Ensure study master files and audit-ready documentation are maintained. People Management Manage statisticians, programmers, and technical staff, overseeing their performance. Coach and mentor staff to achieve excellence. Handle hiring, onboarding, and integration of new team members. Provide technical leadership and More ❯

on business needs. Technical Review clinical trial documents such as protocols, SAPs, CRFs, and CRSs. Author, review, and approve study TFL shells and dataset specifications. Develop, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices. Identify data issues and outliers. Complete, review, and approve CDISC Validation reports. Address data and standards issues appropriately. Stay … informed about emerging standards and their impact on trials. Maintain proficiency in SAS and stay updated on developments. Ensure study master files and audit-ready documents are maintained. People Management Manage statisticians, programmers, and technical staff, overseeing their performance. Coach and mentor staff to achieve excellence. Handle onboarding and integration of new staff. Provide technical leadership and coaching. Project More ❯

based on current business needs. Technical Review 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, adhering to good programming practices. Identify data issues and outliers. Complete, review, and approve CDISC Validation tool reports. Identify and resolve or escalate … data and standards issues as appropriate. Stay aware of emerging standards and their impact on ongoing and future trials. Maintain proficiency in SAS and stay updated with developments. Maintain study master file documents and other audit-ready documents. People Management Line management of statisticians, programmers, and other technical staff, responsible for their overall performance. Provide coaching, mentoring, and support 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 audit-ready documents People Management Line management of statisticians, programmers, and other technical staff, responsible for their overall performance Provide coaching and mentoring to achieve More ❯