Senior Veeva Vault RIM Consultant - Regulatory Transformation

About the role

A senior Veeva Vault RIM specialist with strong pharmaceutical regulatory technology experience is sought to provide independent advisory support for a major regulatory transformation programme. The consultant assesses implementation approaches, dependencies, risks and key technology decisions around Veeva Vault RIM and the wider regulatory technology landscape.

Key responsibilities

• Provide an independent assessment of the Veeva Vault RIM implementation strategy and evaluate phased, staggered and big-bang options
• Assess regulatory, migration and cross-release dependencies, and document options, risks and trade-offs
• Review configuration and integration considerations, and assess MDM, testing, validation and business-readiness dependencies
• Support regulatory transformation and release-readiness assessments, and give input into cutover and go-live readiness
• Work with Regulatory Affairs, IT, system integrators and technology partners, and contribute to governance and executive decision materials

Required profile

• Valid Veeva Vault certification relevant to the services
• Significant enterprise-scale Veeva Vault RIM implementation experience
• Senior-level experience in pharmaceutical/life sciences and strong regulatory technology transformation experience
• Experience in GxP-regulated environments and with large-scale data migration or legacy regulatory-system transformation
• Must be available to attend Basel during planning, governance, validation, cutover and go-live phases

Required skills

• Veeva Vault RIM, configuration, integrations, MDM, testing and validation
• Programme dependencies and release management
• Ability to produce clear recommendations and executive-level decision materials
• Desirable: previous Novartis experience, Freeway or comparable platform transformation, eCAR/ICE governance, and Dragon or comparable legacy systems