Regulatory Professional – Veeva RIM

Novo Nordisk

Regulatory Professional driving continuous optimisation of Veeva RIM submission and registration processes in a global healthcare company. Engaging stakeholders for effective regulatory solutions in a dynamic environment.

Posted 5/27/2026full-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, an analytical and quality mindset, and a flair for IT
Fluency in English, both written and spoken
Experience working with Veeva RIM or a similar Registration Information Management system (nice to have)

Benefits

Comp & perks

Salary package may include short-term and/or long-term incentives
Employee benefits based on position level, location, functional area and relevant market benchmarks

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