- Tustin, CA
What you'll be doing
- Help develop study protocols for the pre-clinical and clinical testing of new products. Assist in the selection of study sites and personnel. Train study participants in all facets of clinical studies. Promote clinical case enrollment to expedite study completion. Monitor and report on clinical performance and of products and study status and outcomes. Coordinate the collection and dissemination of clinical study data. Facilitate training of company sales personnel and distributors. Develop and conduct CME programs as needed to support product/clinical education. Assist RA/QA in analyzing and reporting on clinical performance issues. Assist marketing in the product position and articulation of clinical features/benefits.
What your background should be
- Ability to effective articulate product concepts, clinical protocols and study design. Able to handle multiple tasks effectively and consistently meet deadlines. Attention to detail, able to work autonomously. Ability to effectively interface with physicians, staff personnel and hospital administration. Ability to effectively interface with engineering, clinical and marketing personnel. Capability and flexibility to travel to hospitals and participate in training/marketing events worldwide. Extensive knowledge of neuro anatomy and physiology. Understanding of clinical study project management.
Required Schooling / Training
- High school diploma
Who is the client company
- Company provides medical device services.
- If you are interested in this position, send your resume to firstname.lastname@example.org