51 to 68 of 68 CDISC Jobs in the UK

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 More ❯

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 More ❯

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 More ❯

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 More ❯

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 More ❯

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 More ❯

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 More ❯

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 More ❯

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 More ❯

clinical trial documents (protocols, SAPs, CRFs, CSRs) Authoring, reviewing, and approving study TFL shells and dataset specifications Authoring, validating, and documenting SAS programs Data issue identification and resolution Reviewing CDISC Validation reports Maintaining proficiency in SAS and awareness of standards Maintaining audit-ready study documentation People Management Line management of statisticians and programmers, coaching, mentoring, onboarding, and technical leadership. Project More ❯

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 More ❯

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 More ❯

data exploration and visualization. Application of statistical methodology and concepts in clinical trial analysis, including experience with R-Shiny apps for data exploration. Advanced knowledge of industry standards including CDISC data structures and a solid understanding of the development and use of standard programs. In-depth understanding of the phases of clinical trials and the drug development process. #J More ❯

and RWE studies is desirable. Proven ability to apply R and R-Shiny for analysis and reporting, with skills in data visualization and wrangling. Knowledge of industry standards like CDISC data structures. Deep understanding of clinical trial phases and drug development process. IQVIA is a leading provider of clinical research services and healthcare insights. Learn more at https:// More ❯

clinical trial results into value dossier and regulatory submission packages Lead development of statistical programs using SAS for regulatory and non-regulatory submissions (pre-defined and post-hoc) Implement CDISC standards as required for project deliverables Conduct QC programming for descriptive and complex studies in RWD Contribute to writing study reports and use of visualization tools for reporting and data More ❯

and functional service provider (FSP) partnerships In-depth understanding of FDA and ICH/GCP regulations and guidelines related to data capture and data management processes; strong familiarity with CDISC standards (CDASH/SDTM), medical dictionary coding, 21 CFR Part 11, and industry best practices Exceptional interpersonal, communication, and organizational skills, with the ability to oversee multiple programs and workflows More ❯

and overall quality in a client-facing capacity (project leadership track only) Advanced/expert-level of project leadership/technical track, respectively, working knowledge of data structures (e.g., CDISC SDTM, ADaM), software development lifecycle and their implementation Strong working knowledge of the types of risks associated with a study and the impact on key parameters, such as study timelines More ❯

creative thinking, attention to detail and empathy for patients to data management, and use these skills to ensure the highest quality trial outcome Bonus: You have experience working with CDISC standards such as SDTM You belong here! If your experience and interests match with some of the above, we want you to apply. What you'll focus on Become an More ❯