Lead global software implementation projects and solution design for Veeva Vault Regulatory (RIM) suite across life sciences customers. Responsibilities include requirements workshops, configuration, submission publishing, project/program management, stakeholder liaison, mentoring, and ensuring compliance/CSV. Role is remote within EU/UK (candidate in Spain/Barcelona noted) and requires travel as needed.

Lead software implementation projects for Veeva Vault RIM (Registrations, Submissions, Publishing) across life sciences customers. Responsibilities include requirements gathering, solution design, configuration, project/program management, stakeholder communication, mentoring, and ensuring compliance and validation. Role is remote (UK-based location listed) with travel as required. Preferred languages: German, French, Spanish, Italian.

Lead configuration and end-to-end implementation of Veeva’s Regulatory suite (RIM) for life sciences customers, including requirements gathering, migration, configuration, validation, and go-live. Requires 8+ years in life sciences/healthcare implementations, experience with regulatory processes and computer system validation, and travel up to ~25–50%.

Join Veeva as a Senior Consultant on Professional Services to design and deliver cloud-based Regulatory Information Management solutions (Veeva Registrations, Submissions, Archive, Publishing). Responsibilities include project planning, requirements gathering, migration, configuration, validation, go-live, and customer liaison. Role is remote within the U.S. (prefer Eastern or Central time zones), requires ~25% typical travel (up to 50%), and calls for 8+ years experience in life sciences or healthcare system implementations.

Veeva seeks a Senior Consultant (Safety & PV SME) to lead end-to-end implementations of Vault Safety, including configuration, solution design, data migration, and integrations. The role is customer-facing, remote, and includes project management, mentoring, and presales support. Candidates must have 8+ years in drug safety/pharmacovigilance with experience on safety databases (e.g., ARISg, ARGUS, Oracle) and be authorized to work in the United States. Travel up to 50%. Base salary listed: $80,000–$200,000 (USD, annual).

Remote U.S.-based Senior Consultant role at Veeva Systems to lead implementation of clinical systems (eTMF, CTMS, Site Connect, etc.) across sponsors, CROs and research centers. Requires 8+ years in life sciences/healthcare, experience in system implementation, validation knowledge, stakeholder management, and travel up to ~25–50%.

Remote U.S.-based Senior Consultant role focused on leading end-to-end implementations of clinical systems (eTMF, CTMS, Site Connect, Study Training, Study Startup, Payments, Disclosures, OpenData Clinical) for sponsors, CROs, and research centers. Responsibilities include project planning, gap analysis, workshops, requirements gathering, configuration, validation, migration, integration, training, and go-live. Requires 8+ years in life sciences/healthcare implementations; typical travel 25% (up to 50%); preference for candidates in Eastern or Central Time Zones. Base pay listed: $80,000–$200,000 USD/year.

Remote, full-time Lead Cloud CRM Consultant based in Hungary. Responsible for leading delivery teams and managing client relationships for Veeva Vault CRM implementations and enhancements. Requires 8+ years of enterprise CRM experience (Veeva, Salesforce, MS Dynamics), strong stakeholder communication, solution architecture and leadership skills. Fluency in English required. Total compensation range provided in HUF.

Veeva is hiring a Senior Consultant in R&D to lead small projects, manage teams (2–3 consultants), drive proposals and practice growth, and solve strategic problems using Veeva software, data, and AI. Requires 5+ years in Life Sciences consulting and domain expertise in clinical operations, clinical data management, regulatory, safety/pharmacovigilance, or R&D strategy. Role is flexible (Work Anywhere) and reports compensation range of $80,000–$200,000 base per year.

Veeva is hiring a Senior Consultant in Commercial Business Consulting based in London. The role requires 5+ years' experience in life sciences consulting, leading small-scale project end-to-end, managing teams of 2–3 consultants, driving proposal/business development, and developing deep expertise in 1–2 commercial functions (go-to-market, brand planning, product launch, omnichannel, segmentation/targeting). Veeva is a Work Anywhere company. Knowledge of Veeva products and experience delivering SaaS or tech-enabled consulting solutions are desirable.

Veeva Systems seeks a RIM Implementation Consultant to guide customers in configuring and deploying Veeva Registrations, Submissions, Submissions Archive, and Publishing. Responsibilities include leading requirements workshops, designing and documenting solutions, prototyping, deployment, and program/project management. Requires 3+ years working with life sciences or healthcare organizations; ability to travel as required. Role is remote within the United States with a preference for Eastern or Central Time.

The role is a Project Manager on the Randomization & Trial Supply Management (RTSM) team, leading client meetings and training, producing and managing deliverables (URS, timelines, communication materials, clinical trial material lists), ensuring timelines are met, facilitating UAT and system setup, troubleshooting delivery issues, and providing Tier 3 on-call coverage. Requires a four-year degree or equivalent, 2+ years project management experience in the clinical trial industry, strong communication, organization, and Microsoft Office skills.

As a Process Expert in Data Operations you will simplify and document curation processes, increase automation (sheets, reports, dashboards), manage change projects across 10+ teams, and upskill teams on process excellence. Requires 3+ years' experience in fast-paced environments, strong conceptual and stakeholder communication skills, and excellent English; data analysis skills (SQL, Python) are desirable.

Lead Veeva's R&D Business Consulting practice for Regulatory, accountable for delivery of large global projects, winning $1M+ engagements, and mentoring consulting teams. Requires 10+ years of R&D Life Sciences consulting experience with deep domain knowledge in Regulatory Operations/Affairs and experience managing senior customer relationships.

Lead Veeva Business Consulting's largest and most complex R&D (Clinical) engagements, drive business development for deals $1M+, manage and mentor consulting teams, develop thought leadership, and advise senior stakeholders on using Veeva software, data, and AI to transform R&D operations. Requires 10+ years of R&D life sciences consulting experience and a bachelor’s degree or higher. Total compensation range listed: 94,000–220,000 EUR.

Senior role leading Veeva Business Consulting's largest global commercial projects: accountable for delivery, owning business development for $1M+ deals, mentoring consulting teams, and advising senior (C‑suite) clients on commercial, launch, and omnichannel strategy in Life Sciences. Requires 10+ years of Life Sciences consulting experience and a bachelor’s degree.

Lead and deliver large, complex global projects in the Commercial practice, owning business development for deals $1M+, managing and mentoring consulting teams, and advising C-suite stakeholders. Requires 10+ years of Life Sciences consulting experience, deep domain knowledge in customer engagement strategy, sales/commercial operations, omnichannel and related areas, and a bachelor's degree or higher. Familiarity with Veeva products and SaaS/tech-enabled consulting is preferred.

Lead and grow a professional services RTSM team (project managers and managed services consultants) focused on implementation and support of Randomization & Trial Supply Management studies. Responsibilities include people management, resource and operational management, establishing RTSM processes and best practices, and collaborating across RTSM teams. Requires RTSM experience, 4+ years of people management, strong communication and problem-solving skills; travel ~5-10%.

Veeva Master Class recruits early-career professionals (3–5 years experience or advanced degree holders) to train as Business Consultants for Life Sciences. Responsibilities include customer communications, workshops, stakeholder interviews, process and data analysis, and delivering operational improvements using Veeva software. Role starts April 2027, requires up to 20% travel, is Work Anywhere (remote or office), and Veeva cannot provide visa sponsorship.

Senior Lead Consultant responsible for managing a multi-phased global implementation program for Veeva Quality Cloud. Duties include program and project management, resource planning, release and IT operations oversight, customer liaison, requirements analysis, adoption roadmaps, mentoring project teams, and advising on industry best practices. Requires 8+ years' experience in IT project/program management or consulting, familiarity with SaaS and GxP, and willingness to travel 25–50%. Must be authorized to work in the EU; employer does not anticipate visa sponsorship.