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POSITION SUMMARY: Manages the design, administration and on-site monitoring of clinical trials sponsored by Second Sight. Supervises CRAs in in-house and on-site monitoring. Oversees adherence to SOPs, GCP, and FDA regulations. Ensures compliance with clinical protocols, overall2/29/2016 Sylmar, CA Save This Job
POSITION SUMMARY: The position is responsible for diverse regulatory functions, including but not exclusive to the development of Medical Device submissions and the implementation of Regulatory Compliance. ESSENTIAL DUTIES AND RESPONSIBILITIES: ? Prepare submissions for US and2/29/2016 Sylmar, CA Save This Job
POSITION SUMMARY: Design and perform basic and applied scientific research to improve patient and device performance. ESSENTIAL DUTIES AND RESPONSIBILITIES: ? Helps determine research priorities that reflect company goals. Provides strategic and technical advice to management on2/29/2016 Sylmar, CA Save This Job