
at Accenture
ConsultanciesPosted 7 days ago
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**Veeva Vault RIM Migration Analyst: Drive Global Regulatory Data Transition** Experienced Life Sciences professional sought for Veeva Vault RIM migration role. Migrate regulatory data across global organizations. Key responsibilities include data analysis, preparation, mapping, quality assessment, and migration support. Collaborate with business SMEs, technical teams, and testing teams. Required skills: 3-6 years' experience in Life Sciences/Pharma, RIM/Veeva Vault knowledge, regulatory data domains expertise, data migration experience, agile methodologies (Jira).
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Full Job Description
We are seeking a RIM Migration Business Analyst to support regulatory data migration activities within Veeva Vault RIM implementation programmes. The role will focus on regulatory data analysis, migration preparation, data mapping, data quality assessment, and supporting migration execution activities across global Regulatory organisations.
The ideal candidate will bring a combination of regulatory domain understanding, migration experience, business analysis capability, and strong collaboration skills.
Key Responsibilities
- Support regulatory data migration activities for Veeva Vault RIM implementations
- Analyse source system data structures, regulatory processes, and data relationships
- Support data mapping, transformation rules, and migration specifications
- Conduct data quality assessments, cleansing analysis, and reconciliation activities
- Support migration testing, validation preparation, and defect management activities
- Work closely with business SMEs, migration leads, technical teams, and testing teams
- Support requirements gathering, user story development, and backlog refinement activities
- Assist with integration and cross-system data flow analysis
- Participate in workshops and stakeholder discussions related to migration readiness and cutover planning
- Support documentation development including mapping specifications, migration protocols, reports, and process documentation
Required Skills & Experience
- 36 years of 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





