11 of 11 Permanent CDISC Jobs in the Thames Valley

reporting tasks. Expert Level (6+ years): Deep expertise in data analytics and clinical reporting. Proven ability to lead projects and mentor teams. Familiarity with CDISC standards and advanced reporting infrastructure. Desired Competencies Strong analytical and problem-solving skills Excellent communication and stakeholder management Experience working in a matrixed, cross-functional More ❯

reporting tasks. Expert Level (6+ years): Deep expertise in data analytics and clinical reporting. Proven ability to lead projects and mentor teams. Familiarity with CDISC standards and advanced reporting infrastructure. Desired Competencies Strong analytical and problem-solving skills Excellent communication and stakeholder management Experience working in a matrixed, cross-functional More ❯

reporting tasks. Expert Level (6+ years): Deep expertise in data analytics and clinical reporting. Proven ability to lead projects and mentor teams. Familiarity with CDISC standards and advanced reporting infrastructure. Desired Competencies Strong analytical and problem-solving skills Excellent communication and stakeholder management Experience working in a matrixed, cross-functional More ❯

reporting tasks. Expert Level (6+ years): Deep expertise in data analytics and clinical reporting. Proven ability to lead projects and mentor teams. Familiarity with CDISC standards and advanced reporting infrastructure. Desired Competencies Strong analytical and problem-solving skills Excellent communication and stakeholder management Experience working in a matrixed, cross-functional More ❯

reporting tasks. Expert Level (6+ years): Deep expertise in data analytics and clinical reporting. Proven ability to lead projects and mentor teams. Familiarity with CDISC standards and advanced reporting infrastructure. Desired Competencies Strong analytical and problem-solving skills Excellent communication and stakeholder management Experience working in a matrixed, cross-functional More ❯

of moderate to high complexity. Responsibilities include data model specifications, data stream integrations, transformation of source to internal data models, and/or creating CDISC submission-ready SDTM tabulation packages (such as aCRF, define.xml, cSDRG). The programmer creates and executes edit check programs, listings, and report solutions to monitor More ❯

lead statistical programming projects, ensuring high-quality, on-time deliverables. This includes developing and validating SDTM and ADaM datasets, performing QC reviews, and ensuring CDISC compliance. You’ll resolve Pinnacle 21 validation issues, review TLFs for consistency, and contribute to regulatory submissions. You'll also create define.xml files, develop and … Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. What in it for you: The opportunity to be involved in a growing More ❯

lead statistical programming projects, ensuring high-quality, on-time deliverables. This includes developing and validating SDTM and ADaM datasets, performing QC reviews, and ensuring CDISC compliance. You’ll resolve Pinnacle 21 validation issues, review TLFs for consistency, and contribute to regulatory submissions. You'll also create define.xml files, develop and … Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. What in it for you: The opportunity to be involved in a growing More ❯

lead statistical programming projects, ensuring high-quality, on-time deliverables. This includes developing and validating SDTM and ADaM datasets, performing QC reviews, and ensuring CDISC compliance. You’ll resolve Pinnacle 21 validation issues, review TLFs for consistency, and contribute to regulatory submissions. You'll also create define.xml files, develop and … Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. What in it for you: The opportunity to be involved in a growing More ❯

lead statistical programming projects, ensuring high-quality, on-time deliverables. This includes developing and validating SDTM and ADaM datasets, performing QC reviews, and ensuring CDISC compliance. You’ll resolve Pinnacle 21 validation issues, review TLFs for consistency, and contribute to regulatory submissions. You'll also create define.xml files, develop and … Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. What in it for you: The opportunity to be involved in a growing More ❯

lead statistical programming projects, ensuring high-quality, on-time deliverables. This includes developing and validating SDTM and ADaM datasets, performing QC reviews, and ensuring CDISC compliance. You’ll resolve Pinnacle 21 validation issues, review TLFs for consistency, and contribute to regulatory submissions. You'll also create define.xml files, develop and … Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. What in it for you: The opportunity to be involved in a growing More ❯