Clinical DB Designer

Responsible for study design, edit specifications and system configurations. The Clinical database designer is accountable for associated quality and timely delivery of assigned study design components in collaboration with other project stakeholders.

Essential Functions
Interprets the study protocol.
Design and update the eCRF.
Create and update Edit Specification Document.
Generate specifications for EDC build components (e. g. , Rights and Roles, System Settings and Home Page)
Complete the Study Authorization Form and Trial Capacity Request Form (InForm)
Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting. Attend and present comments at the Internal Design Review Meeting.
Facilitate the internal Edit Specification Review Meeting and leads the discussions regarding the Edit Specification Document.
Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has appropriate access for Entry and Upd

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs. iqvia. com