R&D - RIM Technology Consultant
On-siteLondon, England, United Kingdom
Job Summary
Support regulatory data migration activities for Veeva Vault RIM implementations by analyzing source system data structures, regulatory processes, and data relationships. Conduct data mapping, transformation rules, and migration specifications while performing data quality assessments, cleansing analysis, and reconciliation. Manage migration testing, validation preparation, and defect management by collaborating with business SMEs, migration leads, technical teams, and testing groups. Gather requirements, develop user stories, and refine backlogs while assisting with integration and cross-system data flow analysis. Participate in workshops regarding migration readiness and cutover planning, and develop documentation including mapping specifications, migration protocols, and reports.
Required Qualifications
- Experience within Life Sciences, Regulatory Affairs, or Pharma R&D programmes
- Experience supporting Veeva Vault RIM implementations or Regulatory migration projects
- Understanding of Regulatory data domains including submissions, registrations, products, and HA interactions
- Experience with data migration, data mapping, reconciliation, or master data management activities
- Experience working with business and technical stakeholders across multiple teams
- Understanding of agile delivery methodologies and tools such as Jira or ALM
- Strong analytical, problem-solving, and communication skills
- Ability to manage multiple priorities within fast-paced transformation programmes
- Veeva Vault RIM certification(s)
- Experience with migration testing and validation activities
- Exposure to R&D platforms such as Veeva Vault Clinical, eTMF, CTMS, or Promomats
- Experience with regulatory compliance or enterprise transformation programmes
- Consulting experience within Life Sciences or regulated environments
- Familiarity with tools such as Jira, HP ALM, Tableau, or migration reporting tools
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