Join Veeva's Safety Professional Services to lead Vault Safety implementations as a project manager and/or solution architect. Responsibilities include requirements gathering, configuration, validation, training, and mentoring. Requires 5+ years in life sciences (majority in Drug Safety/Pharmacovigilance) and 3+ years in technology consulting. Total compensation listed: 750,000–1,250,000 DKK.

Join Veeva's Safety Professional Services to lead Vault Safety implementations as a project manager and/or solution architect. Responsibilities include workshop delivery, requirements gathering, configuration, validation, training, and mentoring. Role requires a minimum of 5 years in life sciences (majority in Drug Safety/Pharmacovigilance) and 3+ years in technology consulting, proficiency in English, fluency in a second language (Italian, Spanish, French, or German), and willingness to travel. Experience with Oracle Argus or ARISg is a plus.

Responsible for leading software implementation projects and solution design for Veeva Vault RIM (Registrations, Submissions, Publishing, Archive) at pharmaceutical and biotech clients. Duties include requirements workshops, configuration, project and program management, stakeholder communication, mentoring, and ensuring compliance with life sciences regulations and computer systems validation. Requires 8+ years implementation experience and willingness to travel.

Senior-level hybrid role focused on driving adoption of Veeva Data Cloud via pre-sales engagements: consultative selling, customer data assessments, product demonstrations, project/team management, and contributing market feedback to the Compass product roadmap. Requires 12+ years in healthcare data/analytics and experience with pharmaceutical commercial data; technical skills include SQL and familiarity with Jira/Confluence.

Senior Director of Solution Consulting focused on driving adoption of Veeva Data Cloud through consultative pre-sales work, customer data assessments, demonstrations, and managing analytics projects and team activities. Requires 12+ years in healthcare data/analytics, deep knowledge of pharmaceutical commercial data products, SQL proficiency, and experience with tools like Jira and Confluence.

Veeva is hiring a Senior Content Application Consultant to join AMS in Hungary (remote, occasional travel to Budapest). The role focuses on Vault PromoMats and Vault MedComms: gathering requirements, performing configuration and data migrations, activating features, troubleshooting, delivering training, and creating reports. Requires 5+ years configuring/supporting software, customer-facing consulting experience, and strong English. Total compensation range listed: 18,000,000–33,000,000 HUF. Veeva does not anticipate visa sponsorship for this position.

Veeva Systems seeks a Senior Implementation Consultant to act as Project Manager for Clinical Operations implementations (eTMF, CTMS, Site Connect, Study Training, Study Startup, Payments). This remote role requires candidates to be based in Copenhagen, Denmark, manage multi‑year implementation programs, lead cross‑functional teams, and have strong English and Danish communication skills; travel as required.

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.

Responsible for analyzing customer requirements and configuring Vault Clinical modules (eTMF, CTMS, SSU, Payments), supporting implementation and post-live governance, troubleshooting, and driving customer adoption and change management. Requires 8+ years implementing/supporting business or IT solutions, in-depth clinical operations knowledge, and fluent English. Total compensation listed: 240,000–380,000 PLN.

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.