Regulatory Professional

Novo Nordisk

Senior Regulatory Professional optimizing Veeva RIM processes and ensuring business value at Novo Nordisk. Engaging with stakeholders and vendors to align with regulatory requirements.

Posted 5/26/2026full-timeSøborg • 🇩🇰 DenmarkMid-LevelSenior💰 DKK 570,200 - DKK 838,100 per yearWebsite

About the role

Key responsibilities & impact

Ensure evaluation, prioritisation, implementation, communication, and training in new Veeva RIM features across Regulatory Affairs
Support and drive Veeva RIM process development and optimisation
Engage with stakeholders and external vendors, providing technical guidance and regulatory input to ensure fit-for-purpose processes and solutions
Guarantee alignment with external regulatory requirements

Requirements

What you’ll need

A Master’s degree in a relevant field, such as science, pharmacy, or equivalent
3+ years of experience in the pharmaceutical or other similar industry, preferably within Regulatory Affairs
Strong understanding of overall business processes, analytical and quality mindset, and flair for IT
Fluency in English, both written and spoken
Nice to have: Experience working with Veeva RIM or a similar Registration Information Management system

Benefits

Comp & perks

Short‑term and/or long‑term incentives
Other employee benefits based on position level, location, functional area and relevant market benchmarks
Opportunities to learn and develop

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Veeva RIMRegulatory Affairsprocess developmentprocess optimisationanalytical skillsquality mindset

Soft Skills

communicationstakeholder engagementtechnical guidancetraining

Certifications

Master’s degree