Study Nurse / Studienassistenz – Neurologie in TZ (20-24 Std./Woche) (m/w/d)
Core
Planning, organizing, conducting, and coordinating interventional and non-interventional clinical trials with pharmaceuticals and medical devices, including participant care and data documentation.
Role type
Study Nurse (Clinical Trial Coordinator)
Builds
Clinical trials from start-up to close-out
Domain
Healthcare / Clinical Research
Required skills
Clinical trial coordination, participant care, vital signs measurement, EKG, laboratory work, data documentation, GCP compliance, protocol/SOP creation, MS Office, digital documentation systems
Preferred skills
Study Nurse certification, practical clinical trial experience, knowledge of national/international regulations, English (verbal and written)
Responsibilities
Coordinate monitoring visits, audits, and inspections; prepare and maintain study protocols and forms; organize study medication; collaborate with internal and external study partners.