Clinical DB Designer

IQVIA India; Bengaluru Urban; Hybrid; INR 800,000 - 1,400,000; Full time

Job summary

IQVIA India is seeking a Clinical DB Designer to design clinical databases, author edit specifications, and configure eCRFs across multiple studies. The role requires collaborating with project stakeholders to ensure quality and timely delivery of study design components.

The candidate will interpret study protocols, design eCRFs, create Edit Specification Documents, and generate EDC specifications (Rights & Roles, Settings, Home Page). Hybrid work across PAN India is offered.

Qualifications

• 3–5 years of experience in clinical data management or database design.
• Experience interpreting study protocols for database design.
• Ability to create and update Edit Specification Documents and study-related forms.

Responsibilities

• Interpret study protocol and design the database to collect required data.
• Design and update the eCRF and Edit Specification Document.
• Generate specifications for EDC components and ensure proper rights and roles.
• Attend and contribute to design review meetings and internal reviews.
• Escalate risks and quality issues and ensure SOP training is up to date.

Skills

Clinical data design

eCRF design

Documentation

InForm knowledge

Tools

InForm

Job description

Job Title : Clinical DB Designer

Experience : 3 to 5

Location : Across PAN India (Hybrid)

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 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 Updates.
• Communicate any project risks to the Data Team Lead, including the potential for missing a timeline in the Data Management Project Plan.
• Escalate potential quality issues.
• Ensure the completion and documentation of all project-specific training, as well as staying current with required Standard Operating Procedures.
• Reviews build timelines and provide input as applicable.
• All responsibilities are essential job functions unless noted as nonessential (N).