10 of 10 CDISC Jobs in Berkshire

and/or Phase III studies. Experience leading oncology studies and knowledge of RECIST is strongly preferred. Experience with creating and validating analysis datasets (CDISC ADaM standard), and Tables, Listings, and Figures. Pinnacle 21 experience is strongly preferred. Expert knowledge of SAS. Professional leadership skills coupled with exceptional communication skills. 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 statistics, programming, and clinical drug development processes. Proficiency in Base SAS, SAS Graph, and SAS Macro. 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 More ❯

using frequencies, histograms) • Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice • Complete and review CDISC Validation tool reports • Ensure the appropriate standards are being applied and adhered to • Familiarisation with simple statistical techniques (e.g. t-test, ANOVA, regression, standard survival More ❯

using frequencies, histograms) • Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice • Complete and review CDISC Validation tool reports • Ensure the appropriate standards are being applied and adhered to • Familiarisation with simple statistical techniques (e.g. t-test, ANOVA, regression, standard survival More ❯

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 More ❯

Clinical Programmer (Data Visualization Expert) to join our FSP Team. Key Responsibilities: Develop, test, and validate clinical data programs and applications. Ensure compliance with CDISC SDTM standards for clinical data. Utilize visualization tools such as Spotfire or other similar tools to create insightful data visualizations. Write and maintain Python scripts … Python programming (PySpark, Databricks, pandas, Numpy) is mandatory for this role. Good SDTM Knowledge. Strong SAS/R Programming and SQL expertise. Proficiency in CDISC SDTM standards. Excellent problem-solving and analytical skills. Strong communication and teamwork abilities. Ability to work independently and manage multiple tasks simultaneously. IQVIA is a 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 ❯