Lead customer-facing implementations of Veeva Network MDM (or similar MDM systems) for pharmaceutical and biotech clients. Responsibilities include data analysis, solution design, high-level platform configuration, integrations to Vault CRM, configuring user portals/dashboards, and coaching junior consultants. Requires 5+ years consulting experience, 3+ years hands-on MDM configuration, willingness to travel ~20–30%, and authorization to work in the United States. Base salary range listed: $80,000–$200,000.

Client-facing Senior Consultant (5+ years consulting) to design and implement Veeva Network MDM and integrations (SQL, ETL, APIs, CSV/FTP). Role includes leading implementations, configuring Vault CRM integrations, running workshops, coaching junior staff, and ~20-30% travel. Must be authorized to work in the United States. Base salary range listed: $80,000–$200,000.

Accountable for the commercial success of Compass Payer by developing and executing go-to-market plans, serving as the customer-facing subject-matter expert on payer data, influencing product roadmap, and enabling sales and marketing. Requires 15+ years of relevant consulting/analytics/commercial experience in life sciences and deep expertise in pharmaceutical payer data and commercial customer engagement.

Partner with global pharma customers to implement Veeva Commercial Cloud products (PromoMats/DAM or Medical). Responsibilities include project delivery (PM / solution architect / functional analyst roles), business process analysis, solution design, stakeholder management, and mentoring internal teams. Requires 6+ years in technology implementation, hands-on experience with Veeva PromoMats, Veeva Vault or Salesforce.com, strong consulting and communication skills, English fluency, and ability to travel. Candidate must be based in Europe and have the legal right to work there.

Senior consultant role at Veeva leading Quality Control strategy and delivery for Life Sciences customers. Responsibilities include leading complex global projects, owning Quality Control business development (targeting $1M+ deals), managing and mentoring consulting teams, driving operating model and laboratory (LIMS) transformations, and advising executive QC stakeholders. Requires 10+ years of Life Sciences consulting experience.

Lead software implementation projects and solution design for Veeva Vault RIM (Registrations, Submissions, Submissions Archive, Publishing) at pharmaceutical and biotech companies. Responsibilities include requirements workshops, configuration, documentation, program/project management, stakeholder liaison, mentoring, and travel as required. Requires 8+ years implementing systems for life sciences, deep knowledge of regulatory submissions and labeling, and experience with computer system validation/compliance.

Veeva seeks an Implementation Consultant to design, configure, and deploy its Vault RIM suite (Registrations, Submissions, Archive, Publishing) for life sciences clients. Responsibilities include requirements workshops, solution design, configuration, prototyping, project/program management, and stakeholder communication. Requires 3+ years in technology implementation services (life sciences/healthcare preferred); travel as required. Total compensation listed: 50,000–110,000 EUR.

Lead technical architect for Veeva Vault CRM and connected solutions, owning implementations and migrations (SFDC to Veeva), advising senior stakeholders, configuring solutions, mentoring teams, and traveling ~20%. Requires 7+ years consulting/architecture experience and fluency in English.

Implement Vault R&D migration projects, including migrating document content and object data from legacy systems to Veeva Vault using Vault API and migration tools; support validation exercises, collaborate with Data Migration Leads and Architects, develop migration tools and contribute to the migration knowledge base. Requires 3+ years with Veeva Development Cloud, customer-facing technical consulting, and implementation/data migration or integration experience; skills in SQL, databases, and REST APIs.

Veeva seeks a Senior Technical Architect for the Patient CRM team to design, document, and implement end-to-end integrations (APIs, middleware, batch) between Patient CRM and external systems. The role is customer-facing, requires ~7+ years of technical consulting/architecture experience in life sciences, strong integration and data-security skills, and may involve up to 25% travel. Base salary range listed: $80,000–$200,000 USD.

Experienced consultant role responsible for leading end-to-end RIM implementation workstreams for MedTech customers, analyzing business processes, acting as primary customer liaison, and developing adoption/enhancement roadmaps. Requires 8+ years in systems implementation or software consulting and 4+ years in Regulatory Affairs/Operations within Medical Device or Diagnostics.

Veeva seeks a Senior Consultant to lead global MedTech RIM implementations, guide customers on regulatory data and document management, analyze business processes, manage stakeholders, and develop adoption/enhancement roadmaps. Requires experience with Veeva RIM or similar solutions, strong knowledge of global regulatory requirements (FDA, EU MDR/IVDR), and domain experience in medical devices/diagnostics. Stated base salary range: $80,000–$200,000 USD per year.

Veeva is hiring a Senior Consultant to lead MedTech RIM implementation workstreams, analyze customer processes, guide adoption of Veeva RIM and industry best practices, and manage stakeholder communication. Requires 8+ years in systems implementation or software consulting, 4+ years in Regulatory Operations/Regulatory Affairs within medical device or diagnostics, and experience with global regulatory requirements (FDA, EU MDR/IVDR) and UDI.

Full-time permanent consultant role on Veeva's Professional Services team focusing on Regulatory Information Management (Veeva Registrations, Submissions, Submissions Archive, Publishing). Responsibilities include requirements gathering, solution design, configuration, deployment, and program/project management. Requires 3+ years' experience in life sciences or healthcare and ability to travel (25–50%).

Senior Lead Consultant responsible for leading a multi-year, multi-phased global implementation program and IT operations for the Veeva Quality Cloud suite. Acts as primary customer liaison, oversees release management, resource planning, forecasting, project governance, and mentors project teams. Requires 8+ years in IT project management/consulting/product management, experience with large enterprise implementations, strong communication skills, SaaS and GxP understanding, and willingness to travel ~25–50%. Must be legally authorized to work in the EU.

Veeva seeks a Consultant/Senior Consultant on the Site Solutions Professional Services team to implement SiteVault (eISF and CTMS), act as primary customer contact, manage long-term customer relationships, support renewals, and provide product feedback. Role is remote within the United States with a strong preference for Eastern or Central Time Zones; typical travel is ~10% (up to 20%). Requires 3+ years of enterprise software implementation experience in life sciences, healthcare, or related fields. Nice-to-have: SaaS/CTMS/eISF management, clinical research site experience, and HubSpot familiarity.

Veeva seeks a Consultant/Senior Consultant for the Site Solutions Professional Services team to lead SiteVault eISF and CTMS implementations, engage with customer stakeholders, support renewals, and provide product feedback. Requires 3+ years of enterprise software implementation experience in life sciences or healthcare; role is remote within the U.S. with typical travel of 10–20%.

Veeva seeks a Principal Business Consultant for its Quality Practice to lead large global projects, drive strategic growth in Consumer Products, manage and mentor consulting teams, and act as a trusted advisor to C-suite stakeholders. Requires 10+ years in management consulting focused on Consumer Products with proven experience winning and delivering $1M+ engagements and deep domain knowledge in Quality, Manufacturing, and Supply Chain.

Serve as a technical pre-sales advisor between pharmacovigilance teams and Veeva's Vault Safety platform: analyze customer challenges, configure and deliver demos, lead workshops and POCs, respond to RFPs/RFIs, and support adoption. Requires 5+ years in life sciences with deep end-to-end pharmacovigilance process knowledge, strong presentation skills, cloud/SaaS familiarity, and willingness to travel (~20–30%).

Veeva seeks a Solution Consultant with 5+ years in life sciences/pharmacovigilance to support sales by designing and demonstrating Vault Safety solutions, running workshops and POCs, responding to RFPs/RFIs, and building relationships with safety stakeholders. Role requires fluency in German and English and ~20-30% travel within the EU.