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# Snr Clinical Database Designer

- **Company:** IQVIA
- **Location:** United States
- **Experience:** Experienced
- **Contract:** Permanent contract
- **Skills:** Databases, System Configuration, Information Technology, Data Management
- **Published:** October 17, 2026
- **Apply:** https://www.healthjobsnationwide.com/node/15588960/apply-external

## About the Role

* Bachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology Req
 * 2-4 years of relevant core Technical designer experience and total exp being 7+ yrs. Req

## Description

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., * 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 meeting. Attend and present comments at the Internal Design Review Meeting. May lead Online Screen 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.
 * Reviews QIP for own projects, identify out of scope activities if any and inform relevant parties.
 * Responsible for multiple study design projects at the same time.
 * Might be working on projects across multiple platforms.
 * Identify areas for process improvements on an ongoing basis. Actively take part and contribute towards process improvement initiatives as assigned besides providing suggestions for continuous improvement of processes.
 * All responsibilities are essential job functions unless noted as nonessential (N).