Remote Validation Lead - Veeva CTMS UAT for Pharma

Consult; United Kingdom; Remote; GBP 83,000 - 129,000; Part time

Job summary

Consult is seeking a Validation Consultant for a remote, long-term contract to support a Veeva CTMS implementation in Clinical Development Operations. The role focuses on business-side validation and UAT, collaborating with Global IT and clinical teams to own the UAT workstream and validation activities.

The candidate will lead the end-to-end UAT process, develop validation docs, and ensure alignment with GxP requirements.

Qualifications

• Experience leading UAT for clinical systems implementations.
• Strong understanding of clinical operations processes.
• Ability to bridge business requirements with IT/validation teams.
• Familiarity with GxP validation standards.

Responsibilities

• Lead the end-to-end UAT process from approach to delivery.
• Develop and maintain validation documentation (URS, etc.).
• Support validation of Veeva CTMS/Clinical Vault environment.
• Translate operations requirements into testing activities.
• Coordinate testing with business users and IT validation teams.
• Ensure activities meet GxP requirements.

Skills

Veeva CTMS

UAT leadership

GxP compliance

Clinical operations

Validation

Tools

Veeva Clinical Vault

Job description

Consult is seeking a Validation Consultant for a remote, long-term contract to support a Veeva CTMS implementation in Clinical Development Operations. The role focuses on business-side validation and UAT, collaborating with Global IT and clinical teams to own the UAT workstream and validation activities.

The candidate will lead the end-to-end UAT process, develop validation docs, and ensure alignment with GxP requirements.