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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
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.