About the role
Monitor clinical trials across Nordic sites for a life-sciences company.
Monitor clinical trials across Nordic sites for a life-sciences company. This is a hybrid role based in Copenhagen, Denmark. The successful candidate will join the clinical team and work closely with senior stakeholders.
Responsibilities
- Monitor trial sites for protocol and GCP compliance
- Verify source data and resolve queries
- Build relationships with investigators and site staff
- Report on site performance
Requirements
- 2+ years' independent monitoring experience
- Strong knowledge of ICH-GCP
- Willingness to travel within the Nordics