Veeva Vault Implementation
End-to-end Vault configuration, requirements definition, and functional delivery for PromoMats and Medical Communications platforms. From scoping through go-live.
Consultant · Commercial Content
AI-driven workflows. Regulated content lifecycle. Enterprise-scale implementation.
Consultant in commercial content implementation for Life Sciences and Biopharma, specialising in Veeva Vault platforms, regulated content lifecycle, and AI-driven workflows for global pharmaceutical and biotechnology organisations.
A supply chain and operations background spanning eight years across European markets brings a delivery-first, operationally grounded approach to every engagement. MBA in Artificial Intelligence, with a practical focus on applied AI in enterprise systems and regulated content processes.
End-to-end Vault configuration, requirements definition, and functional delivery for PromoMats and Medical Communications platforms. From scoping through go-live.
Medical, legal, and regulatory review process architecture, remediation, and optimisation — aligned to global compliance requirements and local market needs.
Design and implementation of AI-driven and agentic automation workflows for regulated commercial content operations at enterprise scale.
SCP digitisation initiatives from process analysis through functional validation, delivering structured medical content management across core biopharma markets.
Design and functional support for API-based integrations connecting Vault platforms to downstream systems and third-party services.
Training programme design, end-user enablement, and adoption support from inception through go-live and beyond.
Designing and implementing AI-driven and agentic automation workflows for pharma commercial content operations.
End-to-end medical, legal, and regulatory review process architecture, remediation, and optimisation for Life Sciences.
Promotional content lifecycle configuration, claims management, and compliant multi-channel distribution for biopharma.
Leading SCP digitisation initiatives across core biopharma markets, from process analysis through functional validation.
Full-cycle platform configuration, environment validation, and go-live support for enterprise Vault implementations.
Eight years leading commercial operations across European logistics — team management, cross-border execution, and process automation.
Aligning AI capabilities with regulated commercial content processes at global scale within a major biopharma programme. Responsibilities span requirements definition, functional design, and cross-functional delivery across a complex, multi-market implementation.
Led cross-market delivery across Phases 0 and 1 of a large-scale medical content migration and SCP digitisation initiative. Delivered process analysis, requirements tracking, and functional validation across core Life Sciences markets.
Enabled compliant digital content distribution across multiple European markets as part of a multi-country biopharma publishing infrastructure programme. Delivered configuration and validation to support compliant, scalable distribution.
Full-cycle ownership from configuration through go-live. Combined platform configuration with training programme design and end-user adoption — delivering full enablement from inception across all workstreams.
Eight years leading commercial operations across European logistics — managing a €78M pipeline, international teams across Spain, Poland, and the UK, and delivering process automation that cut response times by 40%. A foundation in data-driven operations, team management, and cross-border execution that informs a delivery-first consulting approach.