Clinical Study Coordinator
Core
Coordinate essential clinical trial activities across Europe to generate high-quality clinical evidence for medical device research.
Role type
Clinical Study Coordinator
Builds
Clinical studies for medical devices
Domain
Medical devices / Clinical research
Deliverable
client delivery
Required skills
Clinical trial administration, GCP compliance, Electronic clinical trial systems, Study documentation management, Site coordination, Invoicing and payment tracking
Preferred skills
Medical device clinical trials, Trial Master Files management, Arterial/venous disease or cardiovascular therapeutic areas
Responsibilities
Support clinical trial activities throughout the study lifecycle (site selection, activation, execution, data collection, closeout), Coordinate study documentation and maintain Trial Master Files, Prepare study meetings and track follow-up actions, Review and process site-related documents and clinical data, Manage study-related invoicing and payment tracking, Develop study communications and reports, Collaborate with Clinical Program Managers and external partners
Seniority
Mid-level, hands-on IC
