Veeva is recruiting for a Master Class Business Consultant role (start Sep 2026) to support and deliver customer-facing engagements in life sciences commercial operations. Candidates should have 3–5 years' experience or an advanced degree, strong communication and problem-solving skills, be process- and data-driven, and be willing to travel up to 20% annually. Veeva cannot sponsor work visas for this position.

Senior role leading a team and acting as primary customer liaison for implementation and IT operations of Veeva Quality Cloud. Responsibilities include program and project management, release management, customer adoption roadmaps, mentoring project teams, and guiding customers on industry best practices. Requires 8+ years' experience, travel (25–50%), and legal authorization to work in the EU; sponsorship is not anticipated.

Join Veeva Professional Services to implement and design solutions across the Vault RIM suite (Registrations, Submissions, Submissions Archive, Submissions Publishing). The role involves requirements gathering, configuration, prototyping, project and program management, and stakeholder communication for life sciences customers. Remote within the UK/EU with required travel.

Joining Veeva Professional Services to implement the Vault RIM suite (Registrations, Submissions, Publishing, Archive) for life sciences customers. Responsibilities include requirements gathering, solution design, configuration, prototyping, deployment, and program/project management. Requires 3+ years in technology implementation services and ability to travel; fluency in one or more of English, German, French, Spanish, or Italian.

Deliver and configure Veeva CRM and Vault implementations for life sciences clients, performing business process due diligence, solution design, client workshops, UAT and training. Role may act as configuration specialist, functional analyst, solution architect or project manager. Based ideally near a Veeva office (Barcelona, London, Paris, Frankfurt, Berlin); remote/onsite flexibility. Requires 3+ years consulting and SaaS implementation experience, fluent English and an additional European language; travel required (~20%).

Owner of complex, multi-functional global R&D Vault implementations and executive liaison across Sales, Product, and Services to ensure customer success, adoption, and growth. Requires 7+ years delivering enterprise pharma/GxP programs (Clinical, Regulatory, Safety), consulting experience with pharma clients, EU/UK work authorization, and up to 25% travel. Total compensation range €140,000–€220,000.

Remote (EU/UK-based) Global Program Manager role owning complex, multi-functional Vault implementations and long-term R&D transformation for strategic pharmaceutical customers. Requires 7+ years of enterprise program leadership in Pharma (Clinical/Regulatory/Safety), executive stakeholder management, global team leadership, and experience with SaaS/GxP environments. Candidates must have legal authorization to work in the EU or UK and be able to travel up to 25%.

Responsible for developing and executing field marketing plans including event and webinar logistics, virtual and industry events, content development and repurposing, digital outreach (LinkedIn, YouTube, Google Ads), and marketing reporting (Marketo, CRM). Requires 4+ years of B2B SaaS/technology marketing experience and proficiency with Microsoft and Google Workspace tools.

Support development and execution of field marketing plans, manage webinar logistics and virtual/industry events, coordinate with product/creative/content/communications teams, assist content creation and social outreach, and support program reporting. Requires 2+ years marketing experience in B2B SaaS or technology, strong communication and organizational skills, and proficiency in Word, PowerPoint, Excel and social media tools.

Lead end-to-end delivery of complex, large-scale global R&D consulting engagements for life sciences customers. Responsibilities include account leadership, managing teams (4+ consultants), overseeing project budgets of $1M+, driving operating model and organizational change, and developing practice IP. Requires 8+ years in life sciences consulting and a bachelor's degree or higher.

Lead end-to-end delivery of large-scale, global Life Sciences engagements focused on Quality (QA/QC) and operating model transformation. Build senior customer relationships, manage teams of 4+ consultants and project budgets of $1M+, and contribute to practice growth and IP development. Requires 8+ years in Life Sciences consulting and domain expertise in Quality, Manufacturing and Supply Chain.

Director role to grow Veeva's cloud-based Laboratory Information Management System (LIMS) in Europe. Responsible for market entry and growth beyond life sciences, building executive relationships, shaping product strategy, coordinating Sales/Services/Product, and driving customer adoption. Requires 8+ years in laboratory informatics or related software and willingness to travel.

Responsible for end-to-end ownership of data pipelines and parts of the Link data processing platform. Work involves JVM-based languages or Python on Spark, cloud software (AWS or GCP), monitoring/observability, and close cooperation with data science for operating ML models.

Member of Veeva Professional Services focusing on Commercial Content (PromoMats, DAM). Responsibilities include business process discovery, translating requirements into solution designs, configuring the application, overseeing build/test/deploy, documentation, and post-go-live activities. Requires 5+ years in consulting/project management or similar, experience with digital content management systems and life sciences customers, ability to travel as required, and fluency in English. Nice-to-haves include experience with Veeva Vault, various DAM/CRM tools, understanding of European regulatory requirements and validation (GxP), and project management certification.

Deliver Veeva Align solutions and own Align implementation/migration workstreams from requirements to deployment. Collaborate with Commercial Operations, IT, and field teams to translate business processes into scalable configuration and data workflows, produce functional documentation and test plans, support change management and user enablement, and drive adoption of Align best practices. Requires 3+ years' relevant experience, experience with CRM platforms (Veeva/Vault, Salesforce or IQVIA), strong analytical and communication skills, and eligibility to work in the EU or UK. Occasional travel for workshops/on-site activities expected.

Veeva is hiring Consultants and Senior Consultants for Clinical Operations to lead configuration and implementation of eTMF, CTMS, Site Connect, Study Training, Study Startup and Payments solutions. Responsibilities include solution design, configuration monitoring, validation documentation, training delivery, and supporting customer success. Candidates should have clinical trials or implementation experience, understanding of content management and compliance, good English communication, and ability to travel. Role is remote within the EU/UK (Spain location listed).

Veeva Systems is hiring Consultants and Senior Consultants to work remotely within the EU/UK on clinical operations implementations. Responsibilities include requirements workshops, solution design, configuration, validation support and documentation, training delivery, and ensuring customer success. Candidates should have clinical trials experience and/or implementation consulting experience with eTMF, CTMS, Site Connect, Study Training, Study Startup, or Payments solutions, an understanding of content management and compliance/validation, good English communication, and the ability to travel as required. Candidates must be legally authorized to work in the EU/UK; Veeva does not anticipate providing visa sponsorship for this role.

Work as a Consultant on R&D Business Consulting projects to reshape operating models, drive organisational change, and deliver measurable business value for biopharma, medtech, animal and consumer health clients. Lead workstreams end-to-end, mentor Associate Consultants, solve complex problems using software, data and AI, and contribute to business development and internal IP. Requirements include 3+ years in life sciences consulting, domain expertise in Clinical Data/Operations, Regulatory or Pharmacovigilance, strong analytical reasoning, and a bachelor’s degree or higher.

Lead end-to-end workstreams in Quality practice to redesign operating models, drive organizational change, and measure business value across Quality Assurance, Quality Control, and Training. Responsibilities include program and project management, problem solving using Veeva software and data, mentoring Associate Consultants, and contributing to practice growth and business development. Bachelor’s degree required; 3+ years experience in life sciences consulting (business/management consulting preferred).

Lead end-to-end project workstreams delivering commercial solutions for life sciences customers (GTM, brand planning, product launches, omnichannel, segmentation). Requires 3+ years in life sciences consulting, strong quantitative and qualitative reasoning, stakeholder communication, and experience mentoring junior staff. Veeva offers flexible Work Anywhere arrangements.