26 to 50 of 68 Veeva Jobs in England

Veeva Systems is seeking a Global Program Manager to own the successful delivery of complex, multi-functional Vault implementations for strategic European accounts, aligning Product, Sales, and Services to maximize customer impact. You will act as the executive sponsor, forge trusted-advisor relationships with IT and business leaders, define ...

experience are not the target profile. Core experience should include:Incentive compensation design and administrationField force design and deploymentSales operations and CRM strategy (e.g., Veeva, Salesforce)Business development and client relationship managementSales force effectiveness Strong understanding of sales operations processes and CRM platforms used in Life Sciences commercial organizations.Demonstrated … discipline such as Business Technology, Information Management, Business Analytics, Operations Management, or an MBA.Comfort with AI-driven analytics tools and digital commercial platforms (e.g., Veeva CRM, Veeva Vault, Salesforce, or comparable SFA/CRM ecosystems); familiarity with Agentic AI or GenAI applications in a Life Sciences commercial context ...

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead. At the heart … Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors. As a Work Anywhere ...

regulatory platforms strategy and collaborates with senior leaders to ensure compliant, scalable technology across GRAS. The role requires deep experience in regulatory operations, Veeva Vault, and GxP environments, with a track record of delivering robust, audit-ready solutions. #J-18808-Ljbffr ...

Veeva Systems, Inc. is seeking an Application Security Architect to provide security guidance to product engineering and IT, design secure solutions, drive security best practices, and establish architecture standards. You will partner with security leads to grow the security program, mentor junior members, present to steering committees and engineering ...

Veeva Systems, Inc. is seeking an Account Partner to grow QuickVault, a scalable cloud application that helps small MedTech companies bring products to market faster. You will own opportunities, meet annual sales targets, and nurture strategic relationships with early-stage customers. You will work cross-functionally with product, marketing ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

metrics, KPIs, trend analysis, and risk-based approaches to assess QMS performance and drive continuous improvement. * Experience with at least one eQMS, such as Veeva, MasterControl, TrackWise, or equivalent. * Working knowledge of Good Documentation Practice and ALCOA+ data integrity principles. * Demonstrated ability to collaborate with cross-functional teams, foster … skills * Intermediate Microsoft Office skills, including Word, Excel, PowerPoint, and Outlook. Non-Essential Qualifications: * Working familiarity with two or more eQMS systems (e.g., MasterControl, Veeva, TrackWise) * Knowledge of computer systems validation (CSV) in the pharmaceutical/biopharma industry * Knowledge of the clinical trial/drug development process and/ ...

Role Veeva Network is a comprehensive Master Data Management (MDM) solution that helps life sciences companies manage critical product and customer data. Veeva OpenData is a customer reference database offering access to more than 16 million healthcare professional and organization profiles. Our solutions enable faster go-to-market … landscape. As our client base continues to expand, we are seeking a highly skilled MDM Technical Architect to lead complex enterprise-level implementations across Veeva Network and OpenData. You will work closely with commercial life sciences customers to design, implement, and optimize robust MDM architectures. This role requires ...

Team: Recent University GraduatesCity: LondonCountry: United Kingdom Veeva Systems is building the industry cloud for Life Sciences to help companies work in a more efficient and connected way. Learn more about our products, vision and values, and status as a public benefit corporation on our website.Consulting is changing … like other firms. Veeva Business Consulting was launched in 2019 and has grown quickly and organically to a global organization of over 400 people. Our team is focused on making the life sciences industry more efficient and effective through software, data, and consulting working together. We expect significant growth ...

Team: Professional ServicesCity: LondonCountry: United Kingdom Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive … growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society ...

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead. At the heart … Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors. As a Work Anywhere ...

Team: Professional ServicesCity: LondonCountry: United Kingdom Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive … growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society ...