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Principal Clinical Database Manager

IQVIA
Location 📍 São Paulo, Brazil
Posted 📅 June 06, 2026
Work Type ⏰ Full time

Position Overview

Job Overview
Responsible for study build & design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. In addition to project deliveries, the role also would be responsible for the project financials from programming shared services perspective.

Essential Functions
• Interprets the study protocol.
• Design and update the eCRF using third party or in house CDMS tools in alignment with industry standards like SDTM, CDASH as applicable.
• 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...

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Job Details

Employment Type
Full time
📊
Category
Mathematical Science Occupations
🏠
Work Arrangement
On-site
📍
Location
São Paulo, Brazil