GQR
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
#J-18808-Ljbffr
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
#J-18808-Ljbffr