Regulatory Data Partner
Novo Nordisk
full-time
Posted on:
Location Type: Office
Location: Søborg • Denmark
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About the role
- Provide first-line support and manage user access for Veeva RIM
- Analyze Veeva RIM data quality issues and resolve inconsistencies
- Manage creation and maintenance of Veeva RIM objects and metadata
- Lead and support process development projects to improve efficiency
- Maintain up-to-date knowledge of internal and external regulatory guidelines
Requirements
- Master’s degree or higher in science, medicine, IT, or a related discipline
- At least 3 years of relevant regulatory experience
- Knowledge of industry-standard regulatory data models like IDMP, XEVMPD, and SPOR
- Strong understanding of master data changes and overall regulatory lifecycle management
- Excellent verbal and written communication skills in English
Benefits
- Opportunities to learn and develop
- Global healthcare company
- Organizational culture built on mutual respect and a willingness to go beyond
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
Veeva RIMdata quality analysismetadata managementprocess developmentregulatory data modelsIDMPXEVMPDSPORregulatory lifecycle management
Soft skills
communication skills
Certifications
Master’s degree