- Undisclosed
- Salary
- 0–2 yrs
- Experience
- Full time
- Job type
About the role
Job Overview 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…
Full details and the application are on IQVIA's careers site.
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