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.
Key responsibilities:
- 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
Key experience:
- 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.
Required Skills
veeva ctms clinical vault uat gxp validation pharmaceutical operations clinical systems
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Validation Consultant employer: Consult
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