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GQR · 4 days ago

Clinical Database Programmer

United States

Contract

Remote

Senior Level

$90/hr - $95/hr

5+ years exp

GQR is seeking a Senior Clinical Database Programmer with hands-on Veeva CDMS experience to support oncology clinical trials. The role involves building high-quality databases, configuring EDC components, and driving user acceptance testing through to go-live.

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Hiring Manager

Bryan Blair

Responsibilities

Build and maintain study databases in Veeva CDMS aligned to protocol/specs

Configure forms, visit schedules, edit checks/rules, and derivations

Lead database development timelines and quality checkpoints

Run and support UAT: test planning, execution, issue resolution, and approvals

Support integrations (ePRO, IWRS, labs) and coordinate technical details

Provide best-practice guidance, documentation, and training to study teams

Qualification

Veeva CDMSClinical trial operationsCRF design standardsCDISC/CDASH/SDTMOncology experienceUAT supportEDC integration

Required

2+ years of Veeva CDMS (or Veeva EDC) experience end-to-end

5+ years in clinical trial operations/data workflows (pharma or biotech)

Strong knowledge of CRF and edit check design standards and documentation

Experience supporting multiple studies at once with strong ownership and follow-through

Oncology experience and/or global Phase I-III trial exposure

CDISC/CDASH/SDTM familiarity and EDC integration experience

Company

GQR

Glassdoor2.9

GQR redefines total talent solutions, offering a bespoke blend of staffing, search, advisory, managed services, and cutting-edge software tailored to every employer's unique needs.

Founded in 2009

Los Angeles, California, USA

201-500 employees