Specialist RIM Data Maintenance
Core
Provide user support for record creation and maintenance in the Regulatory Information Management (RIM) system for a global portfolio of pharmaceutical products.
Role type
Specialist Regulatory Information Management (RIM) Data Maintenance
Builds
Application-level and Master Data level records in the Veeva Registrations system
Domain
Pharmaceutical industry / Regulatory Affairs
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Data entry, data cleansing, data compliance checks, system workflow management, SOP development, bulk data updates, system improvement proposals
Preferred skills
Regulatory Affairs experience, Regulatory Operations experience, Pharmaceutical industry experience
Technologies
Veeva Registrations (RIM)
Responsibilities
Partner with Regulatory teams on record creation and revision; address user queries regarding field definitions and data standards; participate in data cleansing operations; evaluate data quality issues via consistency checks; support bulk updates; submit dictionary update requests; propose system process improvements; contribute to SOP and user manual development
Seniority
Specialist, hands-on IC
