The role is a Customer Success Manager responsible for acting as a trusted advisor and Pharmacovigilance (PV) expert for large global life sciences customers post-implementation of Veeva Pharmacovigilance applications. Responsibilities include relationship ownership, strategic guidance, creating customer roadmaps, product enablement, and cross-functional collaboration with Sales, Product, Services, and Strategy teams. Requires 7+ years in Pharmacovigilance, experience with large global pharmaceutical companies, and customer-facing consulting experience. Veeva Vault and PV software/SaaS experience are listed as nice-to-have.

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 Consultant role based in Poland (Warsaw preferred). Partner with customers to align business processes with Veeva Vault, lead requirements gathering and system configuration, manage build/test/deploy activities, and support product adoption across Clinical, Safety, Quality, or Regulatory products. Requires 3+ years of software/technology consulting or admin experience and fluent English. Travel under 10%. Total compensation range: 160,000–265,000 PLN per year.

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%.

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).

Join Veeva's Global Medical Consulting practice in Berlin to lead workstreams and transform Medical Affairs operating models using Vault Medical and related products (e.g., Link, CRM). Responsibilities include end-to-end project delivery, mentoring Associate Consultants, driving practice growth, and delivering measurable business value. Requires 3+ years in Life Sciences consulting and a bachelor's degree. Total compensation range listed: 63,000–95,000 EUR (total compensation).

Veeva seeks a Product Expert to support Submissions, Submissions Archive, and Publishing within Veeva RIM. The role requires 3+ years in regulatory operations/affairs and consulting or similar customer-facing experience, hands-on knowledge of submission publishing, document management and electronic submissions, and the ability to translate customer needs into product problem statements and roadmap input. Role is Europe-based (UK/London listed), flexible Work Anywhere arrangement, and requires up to 15% travel.

Role to provide subject-matter expertise and customer advocacy for Veeva RIM Submissions, Submissions Archive, and Publishing. Responsibilities include educating customers, gathering and prioritizing feedback into problem statements, contributing to roadmap and release communications, and cross-functional support. Requires 3+ years in regulatory operations/affairs and 3+ years in consulting or related customer-facing roles; willingness to travel up to 15%. Total compensation range listed: 70,000–140,000 EUR.

Join Veeva as a Senior/Solution Consultant on the Veeva Quality team to translate life sciences quality and manufacturing requirements into Veeva Quality solutions. The role is customer-facing across the sales cycle (discovery, demos, workshops, POCs, RFP responses) and requires 5+ years' experience (including 3+ years in solution consulting), strong knowledge of quality/manufacturing in life sciences, Cloud/SaaS experience, and proficiency in English and Hindi. Candidates should be based in or able to work from Mumbai, Hyderabad or Bangalore and willing to travel ~20–30% within India.

Customer-facing Senior Solution Consultant role within Veeva Quality in India. Requires 5+ years' experience (including 3+ years in solution consulting), domain knowledge of life‑sciences quality and manufacturing, SaaS/cloud familiarity, and delivery of demos, workshops and proof‑of‑concepts. Willingness to travel ~20–30% within India.

Customer-facing Senior Solution Consultant for Veeva Quality responsible for translating life sciences quality and manufacturing needs into Veeva cloud solutions. Tasks include discovery, solution design, demos, workshops, POCs, RFP/RFI support and executive engagement. Requires 5+ years' experience (including 3+ years in solution consulting), domain knowledge of quality/manufacturing in regulated industries, and willingness to travel ~20–30% within India.

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.