Sr Clinical DB Designer

IQVIA Argentina; Ernakulam; On-site; INR 600,000 - 980,000; Full time

Job summary

IQVIA Argentina in India seeks a Clinical Database Designer to design study databases, update eCRFs, and ensure timely delivery of design components in collaboration with project stakeholders.

The role covers protocol interpretation, EDC specifications, form completion, and active participation in design reviews. Ideal for candidates with 5+ years in clinical data design and a solid technical background.

Qualifications

• Bachelor's degree in science, CS/IT, or engineering is required.
• 0-2 years of relevant core technical designer experience; total experience around 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 Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting; present comments at Internal Design Review Meeting.
• Facilitate the internal Edit Specification Review Meeting and lead 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 project risks to the Data Team Lead, including potential timeline risks.
• Escalate potential quality issues.
• Ensure training completion and staying current with required SOPs.
• Reviews build timelines and provide input.

Skills

Bachelor's Degree in Science/CS/IT or

Core technical designer experience

Education

Bachelor's Degree in Science/CS/IT or Bachelor in Technology

Job description

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).

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. Req

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.