Sr. Specialist (Data Support End User Expert – Veeva RIM)

Smartedge’s Client is looking for an individual to help with their Sr. Specialist (Data Support End User Expert – Veeva RIM) @ 100 % Remote Working (EU) Job Description : The Sr. Specialist, Data Support End User Expert, is responsible for overseeing global regulatory master data management operations, ensuring data quality, compliance, and adherence to MDM standards within RIM systems. The role leads and supports the data management team, drives process improvements, manages client relationships and governance activities, and develops reporting metrics to ensure timely, accurate, and high-quality service delivery. Leveraging expertise in Regulatory Affairs systems, data governance, reporting, and Six Sigma methodologies, the individual enables operational excellence and continuous improvement across regulatory data management processes.Support Veeva Active Dossier Management by performing:Dossier Lifecycle Oversight: Maintain a holistic, cross-market view of current, submitted, and superseded product documents using Veeva Vault Active Dossier.Data & Process Automation: Oversee automated generation and calculation of dossier records linked to regional submissions, global content plans, and health authority interactionsConfiguration & Maintenance: Manage Active Dossier templates, object lifecycles, and country-level generation rules within Veeva Vault.Cross-Functional Support: Partner with regulatory authors, CMC teams, and submission managers to verify traceability and resolve document-type discrepancies.Audit & Compliance Readiness: Ensure accurate tracking of local-language translations, source files, and status history across various international markets. Key Responsibilities:Responsible for guiding the entry, updating, maintenance, and archival of data entry/correction requests from RIM system users globally Helps establish MDM standards to enable the transfer of information from data entry request forms into the established systemsEnsures sustained data qualityActs as the liaison to client management for all process-related itemsEscalates issues and concerns from team membersConveys feedback from the client to team membersResponsible for establishing and providing oversight to the data management team, ensuring that:Team members are trained appropriately and understand their rolesService levels are metAll deliverables are produced according to the process and within the agreed timelinesAssist in identifying process improvement areasParticipates in governance meetings with the client regularlyWorks with the client to develop a clear and detailed plan for reporting metrics Required Skills & Experience:Experience in developing and maintaining master data management standards for regulatory systemsAbility to handle transactions in line with the established procedures and policies Ability to handle project operations Ability to protect confidential information Strong capacity to work within deadlines Ability to perform the assigned tasks swiftly and accurately Detail oriented Outstanding skills in customer service delivery Demonstrated problem-solving skills Proven experience in analyzing information in support of data management activities Managing processes and ensuring staff compliance Experience in Six Sigma methodologyExperience in supporting and working with tools and systems used in the Regulatory Affairs environment Developing standards Reporting skills Expertise in regulatory and data reporting systems and MS Excel Key Requirements:Experience in pharmaceutical, biotechnology, or medical device organizations operating globally. Bachelor’s degree required.Experience leading data governance, master data management, process improvement, or transformation initiatives.Familiarity with reporting, analytics, and data visualization tools. If this sounds like a role you would be interested in or if you know someone in this field. Connect with me or email me at pavitra.b@smartedgesolutions.co.uk Alternatively, you can call me on Tel: +44(0)203 500 2108.