IQVIA in Reading, UK, seeks an experienced CDISC standards expert to shape the end-to-end design of client standards aligned to CDISC and regulatory guidance. You will provide guidance and training to IQVIA clients and internal teams, ensuring adherence to FDA submission requirements.
You will mentor staff, develop global tools to support project programming needs, and spearhead productivity tool adoption to improve compliance, efficiency, and timeliness of deliverables.
#J-18808-Ljbffr…
