Contract Conditions:
Start date: ASAP
Location: Europe (Remote)
Interviews: As soon as possible
Language: English
Project: Medical Device, Neurology
Key Responsibilities:
Developing training materials and a procedure manual for our clinical protocol
Conducting in-depth training sessions for all EU sites and physicians involved
in the trial
Attending as many relevant clinical procedures as possible and providing
feedback and support
Liaising with engineers, regulatory authorities, and other stakeholders
Requirements
Strong (5 years or similar) experience in the Clinical field working on Medical Devices
International experience with pre-market clinical studies in the EU
Ability to travel frequently in the EU and occasionally in the US
Master's degree or equivalent ideal
If this role is of interest to you, please apply directly to learn more about the role. If not feel free to share with your network.
