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As a Clinical Research Associate, you will be responsible for monitoring clinical research conducted at investigational sites to ensure compliance with study protocols, applicable regulatory requirements, the policies of the ethics committee, and Medtronic procedures. You will work closely with Medtronic study management teams as well as site staff to resolve issues and ensure the smooth conduct of clinical studies. You would ideally be based in the Netherlands.
Responsibilities may include the following and other duties may be assigned:
Required Knowledge and Experience:
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
At Medtronic, no matter your role, you contribute to technologies that transform lives. You will be shaping the future of healthcare technology and defining the next generation of breakthroughs in care.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job, and employees are expected to comply with all credentialing requirements at the hospitals or clinics they support.
Medtronic is a global healthcare solutions company operating in approximately 160 countries. We are committed to improving lives through our medical technologies, services, and solutions.