8 of 8 Permanent CDISC Jobs in the South East

visualization tools. Proven ability to manage multiple projects and coordinate with external vendors. Mastery of SAS programming for clinical trial data analysis. Knowledge of CDISC standards and regulatory submission requirements. Strong problem-solving skills with a focus on automation and process improvement. Ability to adapt to a fast-paced, dynamic More ❯

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 ❯

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 ❯

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 ❯