Sr Clinical DB Designer

IQVIA LLC; Ernakulam; On-site; INR 700,000 - 1,100,000; Full time

Job summary

IQVIA LLC in Kochi, India seeks a Sr Clinical DB Designer to oversee study design, eCRF updates, and the creation of Edit Specifications. You will coordinate with project stakeholders to ensure timely, quality delivery of design components within the InForm environment.

Responsibilities include interpreting protocols, building database structures, coordinating with Data Management, and ensuring trainings are completed per SOPs. This is a full-time role based in Kochi.

Qualifications

• Bachelor's Degree in Science, Computer Science, Information Technology, or Bachelor in Technology.
• 0-2 years of relevant core Technical designer experience; total experience 5+ years.

Responsibilities

• 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.
• Facilitate the internal Edit Specification Review Meeting and lead discussions on the Edit Specification Document.
• Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has access for Entry and Updates.
• Communicate project risks to the Data Team Lead and escalate potential quality issues.
• Ensure completion of all project-specific training and stay current with SOPs.
• Reviews build timelines and provides input.

Education

Bachelor's Degree in Science/Computer science/Information Technology or Bachelor in Technology

Job description

## Sr Clinical DB DesignerApply: Kochi, India: Full time: Posted Today: End Date: October 12, 2026 (18 days left to apply): R1536965Job 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).Qualifications • Bachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology Req • 0-2 years of relevant core Technical designer experience and total exp being 5+ yrs. ReqIQVIA 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