Validation Consultant

Remote
- Contract
- Start:
Late October / Early November

I'm currently supporting a global pharmaceutical organisation looking for an experienced Validation Consultant to support a major Veeva CTMS implementation within Clinical Development Operations.

This is a business-side validation and UAT role
, rather than a traditional IT/CSV position. The consultant will work closely with Clinical Development Operations and Global IT, taking ownership of the UAT workstream and supporting the wider validation activities for the implementation.

• Lead the end-to-end UAT process
  , including approach, planning, preparation, execution and delivery
• Develop and maintain validation documentation including URS, Traceability Matrices, Master Validation Plans, Risk Assessments, Design Specifications and UAT scripts
• Support the validation of the Veeva CTMS / Clinical Vault environment
• Translate clinical operations requirements into appropriate testing and validation activities
• Coordinate testing activities and work closely with business users and IT validation teams
• Ensure validation activities are completed in line with GxP requirements

• Previous Veeva CTMS or Veeva Clinical Vault experience
• Strong pharmaceutical / life sciences experience
• Hands-on experience leading UAT for clinical systems implementations
• Strong understanding of business requirements and clinical operations processes
• Comfortable acting as the link between business and IT/validation teams

This is a fully remote, long-term contract
, with an anticipated start in late October/early November and potential to run through to the end of 2027
.

veeva ctms clinical vault uat gxp validation pharmaceutical operations clinical systems