4 of 4 CDISC Jobs in the South East

Understanding of data integrity principles, including ALCOA++. Understanding of clinical data management processes, including query management, coding, reconciliation and database lock procedures. Knowledge of CDISC standards, with awareness of SDTM terminology, is desirable. Understanding of risk-based quality management principles and clinical trial operations. Skills & Competencies Strong ability to build ...

role within IQVIA lends itself to a technically minded person with strong communication skills and SDTM knowledge. Having experience in Study Design, CRF annotation, CDISC standards, Vendor management with SAS programming skills will be key for this position. The role can be based remotely from anywhere in Europe ...

Summary: This position is responsible for the development of the end to end design of client standards and study specifications that align to the CDISC standards and regulatory agency guidance's. This position provides this guidance and training to clients of IQVIA. Job Responsibilities: Support clients and IQVIA … authority in the use of CDISC Standards through communication, collaboration, training, and mentorship. Partner with project statisticians and programming teams to develop global tools to support project programming needs in the use of CDISC StandardsLead the implementation of productivity tools for IQVIA and clients which improve compliance, efficiencies, and timeliness ...

making sure they are complete, accurate, and delivered on time. You will configure study structures, repositories, datasets, reporting components, and access in line with CDISC and governance requirements. You will manage role-based access, study configurations, and Git/Azure DevOps resources using approved requests and compliant processes. You will … trial results generation, reporting, and submission processes. You have experience supporting Statistical Computing Environments, including process flows, user access, and Biometrics requirements. You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and Listings. You have worked in regulated pharmaceutical environments and understand SDLC, validation, audit ...