We're hiring a Veeva Clinical Vault Configuration Specialist to lead configuration and delivery across CTMS, eTMF, and SSU for our life sciences clients. You'll own the build — from data model design to workflow configuration to go-live support — ensuring solutions are standard, upgrade-safe, and aligned to Veeva best practices.

Key Responsibilities
Configure Vault CTMS, eTMF, and SSU applications based on client requirements — object models, page layouts, lifecycles, and workflows.
Design cross-application configuration across the Study–Country–Site hierarchy, including milestone-to-document linkages between CTMS and eTMF.
Set up document types and expected document rules within eTMF.
Configure CTMS milestones, monitoring visits, protocol deviations and SSU activity/dependency workflows for site start-up tracking with Country-specific regulatory/IRB submission tracking.
Manage global directory, security profiles, roles, and sharing rules in line with GxP and least-privilege principles.




Translate business requirements into configuration specifications with explicit traceability.
Support UAT, validation and Vault Loader-based data migrations.
Assess the impact of Veeva's tri-annual releases on existing configurations and support regression testing.

Required Skills
3–6 years of hands-on Veeva Vault Clinical configuration experience across at least two of: CTMS, eTMF, SSU.
Robust grasp of the Vault Clinical Data Model and standard clinical features in CTMS, eTMF and SSU is a must.
Working knowledge of the TMF Reference Model and clinical trial operations (site start-up, monitoring, milestone tracking).
Familiarity with GxP requirements (21 CFR Part 11, ICH GCP E6(R2)) as they apply to system configuration.
Experience with Vault Loader/VQL for data migration.

Positive to Have
Veeva Vault certification (Platform).

Exposure to Vault Connections (CTMS–eTMF) or Vault APIs.

📌 Configuration Specialist Chennai
🏢 Lorven Technologies
📍 Chennai