Regulatory Affairs Specialist - Contractor- Danish speaker- Remote

Worldwide Clinical Trials(1 month ago)

HybridFull TimeMedior$99,547 - $132,370 (estimated)Regulatory Affairs

About this role

A Regulatory Affairs role within a global CRO focused on supporting regulatory submissions and compliance for clinical trials, with specific responsibility for Denmark under the EU-CTR. The position contributes regulatory intelligence, advises project teams on strategy, and helps maintain country-specific regulatory documentation and labeling. It supports cross-regional submission activities and stakeholder communication.

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Required Skills

Regulatory Submissions
Submission QC
Translation Review
Labeling Maintenance
Regulatory Intelligence
ICH GCP
Project Management
Microsoft Office
Risk Mitigation
Stakeholder Communication

Qualifications

Degree in Medical, Biological, Physical, Health or Pharmacy Science

About Worldwide Clinical Trials

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Worldwide Clinical Trials is a top-rated, full-service global CRO. We provide 30+ years of clinical expertise to benefit your study. Learn more about us here.

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