Teams at NAMSA

Manage and monitor clinical (medical device) study sites to ensure participant protection and GCP/regulatory compliance. Perform on-site and remote monitoring, site start-up and close-out activities, document and metrics management, training, safety support, regulatory submissions, and liaison with investigators and project teams. Role is field-based with high travel and requires French fluency.

Manage MedTech projects end-to-end as the client liaison: define scope, plan schedule/budget/resources, ensure quality and QS compliance, run project setup and closure, handle financials and change orders, support audits and CAPAs, and drive project management best practices while mentoring team members.