Full-time, permanent remote Senior Consultant role at Veeva focusing on Veeva Vault and related products (Clinical, Safety, Quality, Regulatory). Responsibilities include engaging customer stakeholders, translating business needs into scalable solution designs, requirements gathering, system configuration, testing and deployment, and advising on platform adoption. Requires 8+ years of software/technology consulting or admin experience and fluency in English. Candidates must reside in Poland and have legal authorization to work; travel is under 10%.

Full-time, permanent remote Senior Consultant role (must reside in Poland) working with Veeva Development Cloud and Veeva Vault. Responsibilities include requirements gathering, system configuration, full-lifecycle delivery, solution design, product adoption, and stakeholder engagement across Clinical, Safety, Quality, or Regulatory products. Requires 8+ years of software/technology consulting or admin experience and fluent English. Travel under 10%.

Veeva is hiring a Senior Consultant (Software) based in Poland to work remotely. The role partners with customers to align business processes with Veeva Vault, lead requirements gathering, perform system configuration, manage build/test/deploy activities, and support product adoption across Clinical, Safety, Quality, or Regulatory areas. Requires 8+ years of software/technology consulting or admin experience and fluency in English; travel is under 10%.

Full-time, permanent remote role based in Poland. Partner with customers to align business processes to Veeva Vault, lead requirements gathering and system configuration, manage build/test/deploy activities, and advise on product adoption. Requires 3+ years software/technology consulting or admin experience and fluent English. Travel under 10%.

Full-time permanent remote role based in Poland. Partner directly with customers to align business processes with Veeva Vault, lead requirements gathering and system configuration, manage build/test/deploy activities, advise on product releases, and focus on Clinical, Safety, Quality, or Regulatory products. Requires 3+ years of software/technology consulting or admin experience and fluent English. Occasional travel under 10%.

Head the customer success and services team for Veeva Ostro (a conversational AI platform for life sciences). Oversee customer implementations and ongoing services, use customer data and analytics to improve adoption, retention and ROI, and collaborate with sales and product on account plans and product improvements. Role is based in Boston, MA; base salary range listed as $200,000–$270,000.

Lead role managing eCOA implementation engagements: providing implementation proposals, scoping and planning projects, negotiating SOWs and contracts, managing partner vendor relationships, and aligning with sales and services teams. Requires 5+ years in consulting/services for clinical data applications and familiarity with clinical data capture systems (EDC, IVRS, CTMS, safety systems).

Lead pre-sales and implementation scoping for Veeva ClinData customers, produce proposals and Statements of Work, align internal and partner teams, and set expectations for successful clinical data application implementations. Requires experience in clinical trial data systems, SOW negotiation, and client-facing consulting (5+ years).

Partner with global pharmaceutical customers to implement Veeva Commercial Cloud (PromoMats/DAM, Medical), lead business process discovery and solution design, oversee build/test/deploy activities, and provide subject-matter expertise. Role is remote (ideally based near a Veeva office in Europe), requires ~20% travel and candidates must have the legal right to work in Europe.

Partner with global pharma organisations to implement Veeva Commercial Cloud products (PromoMats/DAM and Medical). Lead discovery, solution design, build/test/deploy activities and provide subject-matter expertise; requires 3+ years in technology implementation roles and fluency in English. Candidate must be based in Europe and Veeva does not handle VISA.

Lead delivery of implementation projects (roles include Project Manager, Solution Architect, Functional Analyst) for Veeva PromoMats/DAM or Medical across pharmaceutical, consumer health, and medical device clients. Requires 6+ years in technology implementation, hands-on Veeva PromoMats/Vault or Salesforce.com experience, strong consulting and stakeholder management skills, fluent English, ability to work remotely, and willingness to travel (~20%). Candidate must be based in Europe and able to work legally where located; Veeva does not handle visas.

Lead implementations of Veeva's MedTech Quality Management solutions, analyze customer processes and requirements, act as primary customer liaison, and guide post-implementation adoption. Requires 6+ years in GMP systems ownership or software consulting and knowledge of FDA, EU MDR/IVDR, ISO 13485/14971 and QMS processes (complaints, CAPA, nonconformance, risk).

Vendor-side, advisory-led role working with Life Sciences customers (from biotechs to global pharma) to design complex platform configurations, drive legacy-to-cloud migrations, influence product roadmaps with R&D, and mentor regional consultants. Requires 8+ years implementing/supporting business and IT operations technology (ideally ECM), prior Veeva Vault or enterprise CRM/cloud experience, and fluent English. Posted location references Hungary (Budapest) and also states a requirement for physical residence in Poland with local work authorization (no visa sponsorship). Total compensation listed: 18,000,000–33,000,000 HUF (annual range).

Join Veeva's CEE hub as a Senior Technical Consultant focused on Veeva Clinical Operations or Veeva Regulatory (Vault). The role requires leading complex platform architecture and migrations from legacy/on-premise systems to SaaS, providing technical mentorship, collaborating with R&D and Product teams, and advising enterprise life sciences clients. Requires 8+ years' experience, fluent English, and legal authorization to work and reside in Poland (no visa sponsorship).

Veeva Systems seeks a Project Management Consultant for its Clinical Data Professional Services team to manage project teams implementing Veeva Clinical Data Suite (EDC, Coder, DQS, etc.). Responsibilities include timeline, budget, and resource management, risk mitigation, vendor oversight, and coordinating cross-functional stakeholders. Requires 2+ years each in project management, software implementation, and life sciences; familiarity with Jira/Smartsheet and clinical data software is a plus.

Veeva Systems seeks a Project Management Consultant (based in Boston, MA) to manage project teams implementing Veeva Clinical Data software (EDC, Coder, DQS). Role requires maintaining timelines, budgets, deliverables, managing resources and vendors, coordinating with clinical data and IT stakeholders, and supporting post-implementation transition. Minimum 2 years’ experience in project management, software implementation, and life sciences. Base salary range listed: $70,000–$140,000 per year.

Join Veeva's Clinical Data Professional Services team as a Project Management Consultant responsible for leading project teams implementing Veeva Clinical Data applications (EDC, Coder, DQS, etc.). Responsibilities include developing and maintaining timelines, budgets, deliverables, risk mitigation, vendor coordination, cross-functional alignment, and supporting transition to post-implementation operations. Requires at least 2 years' experience in project management, software implementation, and the life sciences industry.

Customer-facing senior role responsible for interpreting legacy clinical databases, performing data transformation and mapping, developing/validating SQL-based scripts and listings, and leading end-to-end migrations into Veeva Vault CDMS and DQS. Requires 5+ years working with EDC and clinical data management, programming experience (SAS, R, Python, SQL), life sciences industry background, and willingness to travel up to 10%. Total compensation listed: 68,000–115,000 EUR.

Customer-facing senior role responsible for end-to-end delivery of clinical data migrations from legacy EDC systems (e.g., Medidata Rave, Oracle InForm) into Veeva Vault CDMS and DQS. Tasks include interpreting legacy database structures and protocols, data transformation and mapping, developing validation scripts and SQL listings, coordinating cross-functional teams, and mentoring junior staff. Requires 5+ years' EDC/clinical data management experience and programming skills (SAS, R, Python, SQL). Based in Budapest, Hungary. Total compensation range provided: 18,000,000–33,000,000 HUF (annual, total comp).

Customer-facing senior role responsible for interpreting legacy clinical database structures, performing data transformation and mapping, developing validation scripts and SQL listings, leading end-to-end migrations into Veeva Vault CDMS/DQS, and providing product feedback and reusable migration tools. Requires 5+ years in EDC clinical software, programming skills (SAS/R/Python/SQL), and life sciences industry experience.