Study Nurse
On-site · Odense, South Denmark, Denmark
Job Summary
Study Nurse role supporting the conduct of clinical trials at a single Odense site. Responsibilities include coordinating patient visits, performing study-related procedures (sample collection, vital signs, ECGs), ensuring data entry and query resolution, handling investigational medicinal products (storage, accountability, dispensing), and providing patient support and training on study procedures. Requires nursing qualification and experience with clinical trials, and a solid understanding of GCP and regulatory processes. The assignment is a low-FTE engagement of a few hours per week at the Odense site, within a global CRO environment.
Required Qualifications
- Degree in Nursing or equivalent healthcare qualification
- Previous experience working with clinical trials as a study nurse or coordinator
- Good understanding of GCP and clinical trial processes
- Strong organizational skills and ability to work independently
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