Regulatory and Start Up Specialist - Nordics
IQVIA · Copenhagen, Denmark
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Role summary
This role manages site activation activities and regulatory compliance for clinical trials across Nordic countries. The specialist serves as primary contact between investigative sites, project teams, and management, ensuring adherence to regulations, SOPs, and timelines while preparing and maintaining regulatory documentation. Candidates should have a life-science background, three years of relevant experience, fluency in Swedish/Finnish/Danish, and expertise in EC/RA submissions and local regulatory requirements.
Privacy & handoff
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