Senior Veeva CDMS Programmer — Oncology Trials (Remote)

GQR; United States; On-site; USD 126,739 - 135,004; Full time

Job summary

GQR is seeking a Sr. Clinical Database Programmer (Veeva CDMS) for an 18-month contract. Remote within the United States. Pay: Low-to-mid $90s/hour (DOE). You will build high-quality databases and configure EDC components, driving UAT through go-live in oncology trials.

You will collaborate with Lead Data Managers and study teams, lead development timelines, and support integrations with ePRO, IWRS, and labs while ensuring robust documentation and training across projects.

Qualifications

• 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.

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.

Skills

Veeva CDMS

Veeva EDC

CDISC/CDASH/SDTM

Tools

Veeva CDMS

Veeva EDC

Job description

GQR is seeking a Sr. Clinical Database Programmer (Veeva CDMS) for an 18-month contract. Remote within the United States. Pay: Low-to-mid $90s/hour (DOE). You will build high-quality databases and configure EDC components, driving UAT through go-live in oncology trials.

You will collaborate with Lead Data Managers and study teams, lead development timelines, and support integrations with ePRO, IWRS, and labs while ensuring robust documentation and training across projects.