Lead pharmaceutical customers in configuration and adoption of Vault Safety within a Managed Services team. Responsibilities include requirements analysis, solution design, configuration, validation, migration, integration, troubleshooting, change management, and working with product teams. Requires 8+ years in Drug Safety/Pharmacovigilance and strong English communication; consulting/customer-facing experience is expected.

Lead configuration and post‑implementation managed services for Veeva Vault Safety customers: gather requirements, design solutions, configure and validate systems, support migrations and integrations, troubleshoot, drive change management, liaise with customers and internal teams, and mentor junior consultants.

Join Professional Services to implement Veeva Vault Safety for biopharmaceutical customers. Responsibilities include leading business workshops, documenting requirements, designing solutions, working with configuration teams, advising on data migration, driving change management for SaaS adoption, and liaising with customers and product teams. Requires 10+ years in life sciences with a focus on drug safety/pharmacovigilance, strong SQL experience, and familiarity with safety systems (e.g., Argus, Aris). Travel approximately 25%.

The Senior Consultant will support assigned RIM customers (post-implementation managed services), configure and implement Veeva Vault solutions, act as a customer liaison, drive change management from on-prem to SaaS, and collaborate with product and internal teams. Role requires proven customer-facing consulting experience, software configuration/implementation experience, fluent English, and at least a bachelor's degree. Position is remote and based in Hungary (Budapest) with total compensation listed in HUF.

Provide post-implementation managed services for Veeva Vault Regulatory Suite customers: gather requirements, configure Vault, advise on best practices, liaise between customers and internal product/implementation teams, and drive change management. Requires experience configuring/supporting software solutions, consulting/customer-facing experience, fluent English, strong communication and presentation skills, and at least a bachelor's degree. Total compensation range listed: 240,000–380,000 PLN. Veeva does not anticipate providing visa sponsorship for this role; candidates must be legally authorized to work in Europe.

Full-time Senior Consultant role supporting life sciences customers in implementing and configuring Veeva Vault Clinical (e.g., eTMF, CTMS, SSU, Payments). Requires 8+ years implementing/supporting IT or business solutions, deep clinical operations process knowledge (ICH-GCP), strong English communication, and experience in consulting/customer-facing roles.

Join Veeva's Professional Services as a Senior Consultant to design, configure, and deploy Veeva’s Regulatory suite (Registrations, Submissions, Submissions Archive, Publishing) across the full implementation lifecycle. Role requires 8+ years in life sciences/healthcare system implementations, experience with validation and regulatory compliance, and typical travel of 25% (up to 50%).

Lead configuration and implementation of Veeva Regulatory products (Registrations, Submissions, Submissions Archive, Publishing). Manage full implementation lifecycle including planning, requirements gathering, migration, configuration, validation, and go‑live. Act as primary customer liaison, mentor consultants, and collaborate with Product, Strategy, and Sales. U.S.-based remote role (preference for Eastern/Central time zones); typical travel 25% (up to 50%). Base salary range listed: $80,000–$200,000.

Lead implementations and deployments of Veeva Vault Quality: analyze customer business processes, design solutions meeting global regulatory needs, configure and deploy cloud-based QMS/LIMS solutions, support data migration and integrations, and mentor junior consultants. Requires 8+ years in IT project management, GMP systems ownership, or software consulting; experience with SaaS, GxP, and life sciences quality/manufacturing. Permanent remote role; base salary range $80,000–$200,000. Veeva does not anticipate providing visa sponsorship for this position.

Remote, full-time Senior Consultant role on Veeva's Professional Services team implementing Vault Quality (QMS/LIMS) for life sciences customers. Responsibilities include business process analysis, translating requirements into solution design, configuration, data migration, systems integration, and customer-facing consulting. Requires 8+ years of relevant IT/project/consulting experience; up to 50% travel; visa sponsorship is not anticipated.

Veeva seeks a Senior Consultant for its Vault Quality product to analyze customer processes, design and configure cloud QMS/LIMS solutions, support data migration and integrations, and serve as a trusted advisor across implementations. The role is full-time permanent, remote (Work Anywhere), requires 8+ years' relevant experience, and may require travel up to 50%.

Senior Consultant responsible for configuring and delivering Veeva Vault Safety implementations for life sciences customers. Requires 8+ years in drug safety/pharmacovigilance, experience with safety databases (e.g., ARISg, ARGUS), defining business processes, solution design, project management, data migration, and systems integration. Remote US role with up to 50% travel; candidates must be authorized to work in the United States.

Lead and deliver Vault R&D migration projects across the EU/UK, owning migration strategy, execution, validation and customer engagement. Requires 8+ years of migration experience, experience with enterprise content systems and Vault APIs, familiarity with Life Sciences regulations (GxP), and up to 20% travel.

Join Veeva as a Migration Architect on the EU Professional Services team to own end-to-end Vault R&D migration projects, advise on ETL and data quality, lead validation/verification, and mentor Data Migration Specialists. Role is remote within EU/UK (Denmark/Copenhagen listed), requires 8+ years of migration experience, 5+ years project leadership, familiarity with Life Sciences regulations (GxP), and up to 20% travel. Total compensation range provided: 750,000–1,250,000 DKK.

Join Veeva as a Migration Architect to own end-to-end migration projects to the Veeva Vault platform, advising on ETL, data quality, validation, and migration verification. Role is remote within EU/UK (location listed as London, UK), requires ~8+ years migration experience, project leadership, and up to 20% travel across Europe. No visa sponsorship anticipated.

Experienced consultant role focused on leading Complaints Management implementations for MedTech customers using Veeva's QMS solutions. Requires experience analyzing customer processes, leading implementation workstreams, liaising with stakeholders, and guiding post-implementation adoption. Requires 8+ years in GMP systems ownership or software consulting and 5+ years in medical device complaints management; strong knowledge of FDA and EU regulations and ISO standards. Veeva Vault experience is desirable. Location: Boston, Massachusetts / Remote US.

Lead QMS Complaints implementation workstreams for MedTech customers, analyze customer processes and requirements, serve as primary customer liaison, and guide post-implementation adoption and continuous improvement. Requires 8+ years in GMP systems ownership or software consulting, 5+ years in medical device complaints management, and knowledge of FDA, EU MDR/IVDR, ISO standards and related regulations.

Remote (US-preferred) Professional Services role responsible for analyzing current-state clinical processes, designing solutions, configuring Veeva Clinical (eTMF, CTMS, Payments, Site Connect, Study Training), and defining roll-out strategies. Requires 8+ years implementing clinical systems, stakeholder management, mentoring experience, and ability to travel up to 50%.

Lead MedTech customers through implementation and deployment of Veeva Clinical applications (eTMF, CTMS, Payments, Site Connect, Study Training). Requires 8+ years implementing clinical systems and processes, experience with process analysis, solution design, data migration, systems integration, stakeholder management, and willingness to travel up to 50%. Role is remote within the United States with preference for Eastern or Central time zones.

Lead MedTech customers through clinical transformation by implementing Veeva Clinical suite (eTMF, CTMS, Payments, Site Connect, Study Training). Responsibilities include analyzing current-state processes, designing solutions, defining roll-out strategies, managing stakeholders, mentoring junior consultants, and supporting data migration and integrations. US-based remote role with preference for Eastern or Central Time Zone; ability to travel up to 50%. Base salary range listed: $80,000–$200,000.