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Veeva EDC Administrator

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Location: Remote
Compensation: To Be Discussed
Reviewed: Thu, Nov 05, 2026
This job expires in: 30 days

Job Summary

To support a pharmaceutical company conducting global clinical trials, the contract Veeva EDC Administrator will configure, support, and enhance the Veeva Vault EDC platform while working remotely during Pacific Time hours.

Key responsibilities
  • Configure and administer Veeva Vault EDC across development, test, and production environments, including study setups and workflows
  • Provide production support for study builds, amendments, and troubleshoot integration errors and system defects
  • Gather clinical requirements and deliver EDC enhancements while maintaining documentation and compliance with GxP/CSV standards
Required qualifications
  • 6+ years of experience in clinical systems, with at least 3 years of hands-on Veeva Vault EDC configuration and administration
  • Experience providing production support in a pharmaceutical, biotech, or CRO environment
  • Strong understanding of clinical trials, clinical data management, and the study lifecycle
  • Familiarity with GxP, 21 CFR Part 11, and computer system validation (CSV)
  • Ability to work during Pacific Time hours

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