1 to 25 of 45 CDISC Jobs in the UK excluding London

Graph). Experience with Containerization such as Docker and EKS/Kubernetes. Experience with one or more RnD research process and associated regulatory requirements. Exposure to healthcare data standards (CDISC, HL7, FHIR, SNOMED CT, OMOP, DICOM). Experience to big data technologies and handling. Knowledge of machine learning operations (MLOps) and model deployment. Strong problem-solving and analytical abilities. Excellent More ❯

Graph). Experience with Containerization such as Docker and EKS/Kubernetes. Experience with one or more RnD research process and associated regulatory requirements. Exposure to healthcare data standards (CDISC, HL7, FHIR, SNOMED CT, OMOP, DICOM). Experience to big data technologies and handling. Knowledge of machine learning operations (MLOps) and model deployment. Strong problem-solving and analytical abilities. Excellent More ❯

/or clinical drug development process Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM) Join IQVIA to see where your skills can take you Global exposure Variety of therapeutic areas Collaborative and supportive team environment Access to cutting-edge and More ❯

/or clinical drug development process • Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro • Language • Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM) Join IQVIA to see where your skills can take you • Global exposure • Variety of therapeutic areas • Collaborative and supportive team environment • Access to cutting-edge and More ❯

and maintaining deep expertise in the various data collection tools applied in the clinical trials such as DTAs, Clinical Data Tools such as LSAF and Pinnacle 21, and in CDISC standards such as STDM, CDASH, Controlled Terminology, and define.xml. Principal Relationships Internal: Align, collaborate, advise, and share best practices with other functions and teams in Therapeutic Areas, Global Development, Regulatory More ❯

documents such as protocols, SAPs, CRFs, CSRs Authoring, reviewing, and approving study TFL shells and dataset specifications Authoring, validating, and documenting SAS programs Identifying data issues and outliers Reviewing CDISC Validation reports Resolving data and standards issues Staying updated on emerging standards Maintaining proficiency in SAS Ensuring documentation is audit-ready People Management Line management of staff, overseeing performance Coaching More ❯

CRFs, and CSRs Authoring, reviewing, and approving study TFL shells and dataset specifications Authoring, validating, and documenting SAS programs following good programming practices Identifying data issues and outliers Reviewing CDISC Validation reports Resolving data and standards issues or escalating as needed Staying updated on emerging standards and their impact on trials Maintaining SAS proficiency and awareness of developments Managing study More ❯

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 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 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 More ❯

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. 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 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 ❯

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 ❯

the results of clinical trials and/or integrated analysis for submission; Experience in constructing technical programming specifications and producing complex, validated SAS programs; Strong experience in working with CDISC standards, including SDTM, and ADaM, and Define xml; Excellent knowledge of applied statistical methodologies; Excellent knowledge of SAS Macro, SAS/SQL, SAS/GRAPH, and SAS/STAT; Good 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 ❯

regarding database specifications and data transfers Qualifications Bachelor's Degree in Statistics, maths, health informatics, data analytics, computer science,or life sciences field SAS Base Certification required; Experience with CDISC SDTM conversion would be an advantage Excellent analytical, written and oral communication skills Entry level positions are available for recent graduates. Training in SDTM and SAS will be provided. Medpace More ❯

SAPs, CRFs, CSRs) Author, review, and approve study TFL shells and dataset specifications Develop and validate SAS programs for datasets, TFLs, and macros Identify data issues and outliers Review CDISC Validation reports Resolve data and standards issues Stay updated on emerging standards Maintain SAS proficiency Ensure audit-ready documentation People Management Line management of statisticians and programmers Coach and mentor More ❯

protocols, SAPs, CRFs, 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 updated on emerging standards and their impact Maintain SAS proficiency and study documentation People Management Line management of More ❯

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 More ❯

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 More ❯