13 of 13 Veeva Jobs in the UK

years in pharmaceutical commercial data Proven track record of building and scaling enterprise grade data and analytics ecosystems across geographies Deep expertise in commercial pharma data assets (IQVIA, Symphony, Veeva, Salesforce, Adobe, etc.) Strong technical proficiency in: Cloud platforms: AWS (preferred), Azure, or GCP Data tools: Databricks, Snowflake, dbt, Fivetran Visualization tools: Tableau, Power BI Version control & CI/ More ❯

Health Informatics, or related field12+ years of experience in pharmacovigilance, regulatory affairs, R&D operations, or platform managementExpertise in safety data systems, regulatory submission processes, and platform technologies (e.g., Veeva Regulatory and Safety, Argus Safety Solutions etc.)Proven leadership in managing cross-functional teams, projects, and vendor relationshipsStrong knowledge of global regulatory requirements (e.g., FDA, EMA, MHRA) and safety More ❯

regulated, multi-site or global organisations. Strong communication skills with the ability to work confidently with scientific and commercial leaders. Desirable Experience with LabWare LIMS, SAP PLM, Teamcenter or Veeva ELN . Understanding of data science, AI/ML or advanced analytics within R&D contexts. Certifications such as ITIL, TOGAF, PMP or Prince2 . More ❯

regulated, multi-site or global organisations. Strong communication skills with the ability to work confidently with scientific and commercial leaders. Desirable Experience with LabWare LIMS, SAP PLM, Teamcenter or Veeva ELN . Understanding of data science, AI/ML or advanced analytics within R&D contexts. Certifications such as ITIL, TOGAF, PMP or Prince2 . More ❯

depth knowledge of Life Sciences domains such - as Patient Services, Commercial, Medical, and Market Access Engagement - to guide design and delivery. Architect scalable and high-performing CRM solutions across Veeva Vault CRM, Salesforce Sales Cloud, Service Cloud, Experience Cloud, Health Cloud, and Life Sciences Cloud. Identify opportunities to apply AI and Salesforce innovations (including Agentforce and Data Cloud) to More ❯

and/or Orphan Drug therapeutic experience Base SAS®, SAS/STAT and SAS/ACCESS software SAS Macro programming language Advanced experience in Database Management, object-oriented programming Veeva set up experience Medidata Rave certification Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a More ❯

experience in a similar role, ideally within commercial IT or life sciences, with a strong track record of delivering major programmes and managing cross functional teams. Extensive experience with Veeva CRM and Veeva Events Management , with exposure to Vault Platform and the Salesforce ecosystem. Strong understanding of field force effectiveness and sales operations processes , with the ability to More ❯

Migration Lead – Veeva (Vault Platform) Location: EU (Remote or Hybrid, occasional travel) Contract: 12–24 months Sector: Life Sciences/Pharma/Biotech About the Role We’re looking for an experienced Migration Lead to support a large-scale Veeva Vault transformation across multiple EU sites. You’ll take ownership of the end-to-end data and document … migration process – from defining the approach to ensuring everything moves smoothly and compliantly into the Veeva environment. This role suits someone who understands both the technical side of data migration and the regulatory context life sciences companies operate in. You’ll be the bridge between business, IT, and third-party partners to make sure the migration is accurate, validated … and delivered on time. Key Responsibilities Lead all aspects of the migration workstream within a wider Veeva programme. Develop and deliver the migration plan, timelines, and validation approach. Oversee data mapping, transformation, extraction, and loading into Veeva Vault. Work closely with Regulatory, Quality, Clinical, and IT teams to ensure business and compliance needs are met. Manage dry runs More ❯

Job Title: Veeva RIMs Specialist – CTA Strategy & Training Location: United Kingdom (Hybrid/Remote) Rate: £40–£50 per hour (Inside IR35) Job Type: Contract – 6-month initial engagement About Us: We are a specialist recruitment consultancy representing a leading Life Sciences organisation focused on Regulatory Affairs and Veeva platform optimisation. Our client partners with global pharmaceutical companies to … enhance RIMs capability, streamline CTA submission strategies, and drive digital transformation across Regulatory Operations. Role Overview: We are seeking an experienced Veeva RIMs Specialist to support the development and execution of CTA strategy and training materials within a regulated environment. This role requires hands-on expertise in Veeva RIMs modules and a strong understanding of regulatory submission processes. … Key Responsibilities: Lead the design and delivery of Veeva RIMs training materials for Regulatory Affairs teams. Support the implementation and optimisation of CTA workflows within Veeva Vault. Collaborate with global stakeholders to align RIMs functionality with business processes. Provide SME guidance on system configuration, data integrity, and end-user adoption. Ensure compliance with regulatory and quality standards throughout More ❯

R&D Partners is seeking a Consultant Veeva Database Programmer to join a leading organization in the life sciences industry. This is a home-based role within Europe, offering an exciting opportunity to work on database programming and management tasks using Veeva CDMS. Please note that to be considered for this role you must have the right to … Responsibilities: Handle database-related tasks throughout setup, maintenance, and database closure activities. Create study documentation such as data management plans and technical agreements. Validate databases for studies built using Veeva CDMS. Perform updates to live databases, ensuring proper testing and deployment. Assist in developing written standards for the use of Veeva CDMS. Key Skills and Requirements: Experience in … database programming, development, or data management with Veeva CDMS. Certification as a Veeva Study Builder is preferred. Strong knowledge and hands-on experience with Veeva CDMS are essential. For more information, please contact Antony Serrecchia . If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our More ❯

evidence-based recommendations. Stakeholder Engagement – Proven ability to manage complex stakeholder environments and build trusted relationships across all business levels. Salesforce & Ecosystem Knowledge – Familiarity with Salesforce Life Sciences CRM, Veeva Vault, Health Cloud, IQVIA, and Data Cloud integration (including Agentforce use cases). AI & Innovation Mindset – Understanding of how AI can enhance design thinking, delivery, and transformation; active engagement … with Salesforce and ecosystem partners.? What You’ll Bring: Deep knowledge of Life Sciences business processes and challenges. Deep knowledge of Salesforce solutions (Veeva CRM, Sales & Service Cloud and a knowledge of Life Sciences Cloud capabilities). Strong understanding of how to apply Salesforce innovations (including Agentforce) to reimagine business processes. Skills in process design, journey mapping, personas, requirements More ❯

looking for a Senior Project Manager with a strong background in the pharmaceutical industry , specifically focusing on commercial operations . The role requires managing projects that involve Salesforce and Veeva implementations, while ensuring adherence to regulatory and compliance standards in the Pharmaceutical sector. Key Responsibilities: Lead and manage commercial projects end-to-end within the pharmaceutical industry Oversee Salesforce … and Veeva initiatives, ensuring timely delivery and alignment with business objectives Ensure compliance with regulatory requirements across all project activities Collaborate with cross-functional teams, including commercial, regulatory, and IT stakeholders Drive process improvements and ensure effective project documentation and reporting Requirements: Extensive experience in Pharma commercial operations Strong expertise in Salesforce and Veeva platforms Knowledge of Pharma More ❯

Job Title: QA Specialist – Document Controller Contract Length: 6 Months Industry: Pharmaceuticals Location: Stevenage Salary: £18-£20 per hour Start Date : ASAP To provide management of the Veeva Quality Docs (VQD) system, the core GxP Documentation System used on site. Key activities: Provide role of VQD Process owner, including acting as superuser and local business administrator (LBA), as well … notices management, capacity monitoring, destruction management and liaison for archive documentation GMP queries. Qualifications & experience: SVQ Level 3: Highers/higher national certificate/apprenticeship or equivalent Experience with Veeva Vault Experience with GMP environments More ❯