Remote, full-time role based in Hungary. The Senior Consultant will lead drug safety/pharmacovigilance customers in configuring and adopting Vault Safety, act as primary customer liaison, contribute to solution design (requirements, configuration, validation, migration, integration, training), troubleshoot issues, and support post-live governance and change management. Requires 8+ years in Drug Safety/Pharmacovigilance and strong English communication skills.

This remote, full-time Senior Consultant position within Veeva's Managed Services Safety team supports pharmaceutical customers on Vault Safety. Responsibilities include requirements gathering, configuration, validation, migration, integration, troubleshooting, change management, and acting as primary customer liaison. Requires 8+ years in drug safety/pharmacovigilance, 4+ years in consulting/customer-facing roles, and fluent English. Total compensation range: 240,000–380,000 PLN per year.

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%.

Join Veeva's Managed Services Regulatory team to support customers using the Vault Regulatory Suite, acting as a customer liaison, configuring and implementing solutions, and guiding adoption and change management. Role requires experience configuring/supporting software solutions, consulting/customer-facing experience, strong English communication skills, and at least a bachelor's degree. This is a remote, full-time position for candidates legally authorized to work in Hungary; the employer does not anticipate visa sponsorship.

Remote Senior Consultant on the Managed Services Regulatory team supporting customers (e.g., large pharma) with Veeva Vault Regulatory Suite. Responsibilities include configuring and implementing Vault features, advising customers on business processes and best practices, acting as liaison between implementation/maintenance teams and product management, and driving change management for SaaS adoption. Requires experience configuring/supporting software (ideally content management), consulting/customer-facing experience, strong English communication, and at least a bachelor's degree. Candidates must be legally authorized to work in Poland; employer does not anticipate visa sponsorship.

Remote full-time role based in Hungary supporting life sciences customers on Veeva Vault Clinical (eTMF, CTMS, SSU, Payments). Responsibilities include requirements analysis, solution design, configuration, validation, migration, integrations, training, troubleshooting, and driving change management. Requires 8+ years implementing/supporting IT/business solutions in clinical operations and fluent English; Veeva does not anticipate visa sponsorship for this role.

Join Veeva as a Senior Consultant in Clinical Operations to configure and support Vault Clinical modules (e.g., eTMF, CTMS, SSU), lead implementations and post-implementation programs, liaise with customers and product teams, and drive change management. Position requires 8+ years' relevant experience, fluent English, and deep knowledge of Clinical Operations and ICH-GCP.

Lead end-to-end implementations of Veeva’s RIM suite (Registrations, Submissions, Archive, Publishing). Responsibilities include requirements gathering, solution design, configuration, validation, go-live activities, project and stakeholder management, mentoring, and cross-functional collaboration. Remote U.S. role with preference for Eastern or Central time zones and typical travel of ~25% (up to 50%).

Veeva seeks an experienced Senior Consultant with 8+ years in life sciences/healthcare to lead RIM software implementations (requirements, design, configuration, validation, go-live). Role is remote within the United States (preference for Eastern/Central time zones) and involves typical travel of ~25% (up to 50%).

Full-time permanent, remote Senior Consultant (Safety & PV SME) to lead delivery of Vault Safety implementations for life sciences customers. Responsibilities include defining business processes and implementation strategies, solution design and configuration, data migration and systems integration oversight, project and stakeholder management, mentoring project teams, assisting presales, and ensuring customer success. Requires 8+ years in life sciences with Drug Safety/Pharmacovigilance experience; up to 50% travel; US work authorization expected.

Join Veeva as a Migration Architect to design and lead end-to-end data and document migration projects to the Vault platform. The role requires ownership of migration strategy, ETL processes, data quality and validation, collaboration with engineering and services teams, and mentoring Data Migration Specialists. Required: 8+ years of data/content migration experience, 5+ years of project leadership/consulting, familiarity with Life Sciences regulations (GxP). Remote within EU/UK with up to 20% travel.

Veeva seeks a Senior Consultant / Migration Architect to design and lead end-to-end data and document migrations to the Vault platform for life sciences clients. The role requires 8+ years of migration experience, 5+ years of project leadership, familiarity with GxP/validation, and up to 20% travel across Europe. Compensation range listed: 750,000–1,250,000 DKK total.

Join Veeva as a Migration Architect to own Vault R&D migration projects, lead ETL activities, ensure data quality and compliance (including GxP/validation), mentor Data Migration Specialists, and collaborate with Services, Product, Sales, and Engineering. The role is remote within the EU/UK (based in the United Kingdom/London location listed), requires 8+ years of migration experience, and up to 20% travel. Veeva does not anticipate providing visa sponsorship for this position.

Lead implementation workstreams for MedTech Complaints management using Veeva Vault, analyze customer processes and requirements, act as primary customer liaison, and guide adoption of industry best practices. Requires extensive experience in GMP systems or software consulting, complaints management for medical devices, knowledge of FDA/EU regulations and standards (ISO 13485, ISO 14971, relevant 21 CFR parts, EU GMP Annex 11), and familiarity with SaaS and GxP principles.

Experienced consultant role to lead Complaints Management implementation workstreams for Veeva’s MedTech QMS customers. Responsibilities include analyzing customer processes, leading implementations, acting as primary customer liaison, and guiding post-implementation adoption. Requirements include 8+ years in GMP systems ownership or software consulting and 5+ years in medical device complaints management, with strong knowledge of FDA and EU regulations and standards (ISO 13485, ISO 14971).

Lead implementations of Veeva Clinical (eTMF, CTMS, Payments, Site Connect, Study Training) for MedTech and related customers. Responsibilities include analyzing current-state processes, designing solutions, defining roll-out strategies, managing stakeholders, mentoring junior consultants, and supporting integrations and data migrations. Role is remote within the U.S. with up to 50% travel.

Join Veeva Professional Services to lead implementations of the Veeva Clinical suite (eTMF, CTMS, Payments, Site Connect, Study Training) for MedTech customers. The role involves analyzing current-state processes, designing solutions, defining roll-out strategies, mentoring junior consultants, and managing stakeholder communications. Qualified U.S.-based candidates only; remote with preference for Eastern or Central time zones. Salary range listed: $80,000–$200,000 base.

Lead MedTech customers through clinical transformation by analyzing current-state business processes, defining future-state solutions, configuring and deploying Veeva Clinical (eTMF, CTMS, Payments, Site Connect, Study Training), and managing stakeholder communication across implementations. Requires 8+ years implementing clinical systems and working knowledge of life sciences compliance. Position is US-remote (preference Eastern/Central) with up to 50% travel.

Join Veeva as a Senior Consultant focused on implementing Veeva Vault LIMS: assess and review features, lead solutioning, configure systems, run workshops, manage projects and escalations, and mentor colleagues. Role is remote (based in/near Boston, MA), full-time permanent, requires 7+ years implementing LIMS and travel for customer engagements (typical ~25%, up to 50%). Base salary range listed: USD 80,000–200,000.

Remote Senior Consultant role implementing Veeva Vault LIMS with responsibility for assessment, design, configuration, workshops, project management, and customer adoption. Requires 7+ years implementing LIMS and travel up to 50%.