Description
The Study Nurse / Study Assistant will organize and conduct clinical studies in accordance with GCP guidelines, support study participants, prepare and follow up study visits, maintain CRF and eCRF documentation, manage blood samples, and collaborate with principal investigators, monitors, and sponsors. The role also supports audits, inspections, and quality assurance. Candidates should have completed training in a medical profession or biology, ideally have clinical-study experience, and be comfortable with digital documentation systems.
