Back to jobsProviding comprehensive administrative and operational support across all clinical trial phases, ensuring efficient and compliant study execution
Managing trial documentation in the Novo Nordisk Investigator Portal, including set-up, maintenance, and archiving in the (e)TMF and Investigator Site Files
Coordinating clinical supply and equipment activities at the country level, including ordering, handling, import processes, and inventory tracking
Supporting regulatory submissions by preparing, translating, and submitting documents to Regulatory Authorities and Ethics Committees
Facilitating site activation activities, including 'Green Light' checks and drug release documentation
Coordinating meeting logistics and follow-ups for local study team meetings, and supporting the preparation of Investigator Meetings
Liaising with Vendor Managers and Payment Specialists to facilitate contracting and site payment activities
Ensuring cross-functional collaboration and clear communication with internal and external stakeholders, including clinical sites
