NAMSA

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.

Supervises the Global Client Success team and manages client interactions through various laboratory submission portals. Coordinates workload distribution, develops training programs, and serves as a liaison between Commercial, IT, and Laboratory Operations.

Leads the business analysis, design, and implementation of clinical operations systems while managing complex deployment activities. Facilitates Agile processes and collaborates with global teams to improve business practices and technical solutions.

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.