Clinical Database Programmer

GQR; California (MO); Remote; USD 123,984 - 137,760; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Disability insurance

Job summary

A clinical research staffing firm is seeking a Sr. Clinical Database Programmer to support oncology clinical trials in a remote capacity. Candidates should possess strong hands-on experience with Veeva CDMS and have worked in clinical trial operations for at least 5 years. You will be responsible for building high‑quality databases and leading UAT through the go-live phase. This contract position offers competitive pay starting in the low-to-mid $90s per hour based on experience.

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.

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.

Skills

Veeva CDMS experience

Clinical trial operations

CRF design standards

Oncology experience

CDISC/CDASH/SDTM familiarity

Job description

This range is provided by GQR. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Sr. Clinical Database Programmer (Veeva CDMS) - 18-Month Contract

Location: Remote (United States) - must support core Pacific / West Coast hours

Pay: Low-to-mid $90s/hour (DOE)

Our client is hiring a Sr. Clinical Database Programmer with hands‑on Veeva CDMS experience to support oncology clinical trials. You will partner closely with Lead Data Managers and study teams to build high‑quality databases, configure EDC components, and drive UAT through go‑live.

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.

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.

Note: This opportunity is with one of our clients and is not a role at GQR.

Seniority level

Mid‑Senior level

Employment type

Contract

Job function

Science

Industries

Biotechnology Research and Pharmaceutical Manufacturing

Benefits

• Medical insurance
• Vision insurance
• 401(k)
• Disability insurance