26 to 50 of 89 Veeva Jobs in the UK

/biotech commercial lifecycle — from pre-launch through loss of exclusivity Familiarity with the Life Sciences data ecosystem: IQVIA, Symphony Health, Komodo, claims data, Veeva CRM, EMR/EHR , and specialty data assets Experience engaging commercial leaders (VP of Sales, VP of Marketing, Chief Commercial Officer) as a peer ...

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 ...

Veeva Systems is seeking an experienced consultant to lead MedTech Complaints implementations at our global MedTech customers. You will guide the transformation of complaints management processes and configure our cloud-based Vault solution to support enterprise-wide compliance. The role is remote and full-time, based ...

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 ...

dashboards for multiple brands and geographies. The role offers a fully remote setup for UK-based candidates and requires strong Power BI, Salesforce and Veeva expertise, plus Python for automation and analytics. #J-18808-Ljbffr ...

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 ...

Veeva Systems is seeking a senior events leader to head Europe’s corporate events program. You will partner with marketing, sales, strategy, and product to plan and execute large customer conferences, internal field kickoffs, and special programs across Europe. You will hire and mentor a team, manage vendors ...

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 ...

standards, data quality thresholds, KPIs, issue escalation and lifecycle controls for regulatory master data.Set strategic business ownership and governance for the RIM ecosystem, including Veeva RIM, Lorenz docuBridge, AMS, xEVMPD/IDMP processes and related integrations, ensuring investment and release priorities support business needs.Define the resource and operating model … data quality KPIs, issue management and lifecycle controls for regulatory master data.Experience shaping digital and data roadmaps, vendor governance and IT-enabled transformation across Veeva Vault/RIM and related regulatory systems.Strong analytical, communication and change management capability, with ability to convert metrics, risks and data quality signals into ...

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/ ...