NAMSA

The role involves providing clinical field support for medical device development and safety testing. The specialist will assist clients throughout the product development lifecycle to advance MedTech solutions.

The role involves providing clinical field support and engineering expertise for medical device development. The specialist will assist clients throughout the product development lifecycle to ensure safety and regulatory compliance.

The role involves managing clinical site monitoring responsibilities to ensure human subject protection and adherence to GCP and regulatory guidelines. Key duties include conducting site visits, managing study documentation, and serving as the primary contact for site investigators.

The Medical Monitor performs medical review and interpretation of adverse events and device deficiencies while ensuring compliance with regulatory requirements and study protocols. They also serve as a clinical and scientific advisor to clients and provide medical input into the design of clinical study protocols.