Medtronic Danmark A/S, Copenhagen
As a CRA at Medtronic You will be:
The responsible person for the oversight of clinical research conducted at investigational sites to ensure compliance with study protocols, applicable regulatory standards, Ethic Committee policies and procedures and business requirements. The role requires monitoring in all cross-business units at Medtronic, e.g. cardiovascular, neuromodulation, diabetes.
You will be responsible for the startup activities (Site qualification visits, submission package, Patient Information Consent etc.) in Denmark with close collaboration with the study teams.
We are looking for a customer focused team player who is a clinical expert and experience working in a team/matrix environment, specialized in clinical site management, study monitoring and local regulations.