Database Programmer - WFH

## About the RoleGQR's client is seeking a Senior Clinical Database Programmer with hands-on Veeva CDMS experience to support oncology clinical trials. This role focuses on building and maintaining high-quality clinical study databases, configuring EDC components, supporting user acceptance testing, and helping drive database development through go-live.The position partners closely with Lead Data Managers and study teams and requires strong ownership, attention to quality, and experience working across clinical trial data workflows.## Key Responsibilities* Build and maintain study databases in Veeva CDMS according to study protocols and specifications.* Configure forms, visit schedules, edit checks/rules, and derivations.* Lead database development timelines and quality checkpoints.* Plan, execute, and support UAT activities.* Resolve UAT issues and coordinate required approvals.* Support integrations including ePRO, IWRS, and laboratory systems.* Coordinate technical details related to clinical data integrations.* Provide best-practice guidance to study teams.* Create and maintain relevant documentation.* Provide training and support to study teams.* Manage responsibilities across multiple studies while maintaining strong ownership and follow-through.## Required Qualifications* 2+ years of end-to-end experience with Veeva CDMS or Veeva EDC.* 5+ years of experience in clinical trial operations or clinical data workflows within pharmaceutical or biotechnology environments.* Strong knowledge of CRF design standards.* Strong knowledge of edit check design standards and documentation.* Experience supporting multiple clinical studies simultaneously.* Experience with oncology clinical trials and/or global Phase I–III trials.* Familiarity with CDISC, CDASH, and SDTM.* Experience with EDC integrations.## Work Arrangement* Remote position within the United States.* Must be available to support core Pacific / West Coast hours.* 18-month contract.* Mid-Senior level.* Science-focused role within biotechnology research and pharmaceutical manufacturing.## Compensation & Benefits* Pay: Low-to-mid $90s per hour, depending on experience.* Medical insurance.* Vision insurance.* 401(k).* Disability insurance.Apply Now