This teammate will be responsible for managing clinical trials sponsored by ViewRay and providing input and oversight on key physician-initiated studies. This role will be responsible for establishing infrastructure required for clinical studies, ensuring CRO support is timely and adequate and visiting clinical trial sites to provide support and drive study completion on time or early. Experience managing clinical trials is required.
This position will report to the Vice President of Clinical, Regulatory and Quality.
Clinical trial project management, in the medical device field
Ensuring on time or early study completion/deliverables
Managing and supporting physician-initiated studies
Education, Experience, Skills
BS/MS/PhD science-based discipline
Five + years’ experience
Clinical trial in the medical device space is required
Building relationships with clinical trial sites, including physicians, coordinators and other staff is required
Physics or MRI experience is useful, but not required
Ability to travel 50%
Creative, flexible, and collaborative in approach to technical problem solving
Ability to communicate effectively, both orally and in writing, at a variety of technical levels with internal teammates and external customers
Being able to professionally represent ViewRay with customers is critical
Driving for results and managing study team members at all levels is required