Jobs at NAMSA

Lead and manage medical device projects across the full lifecycle: staffing, planning, budgeting, scheduling, risk management, client liaison, regulatory and quality compliance (QS/GLP/GCP/GMP), project setup and closure, metrics/reporting, and lessons learned. Support audits, change orders, and mentor team members while driving PM best practices and continuous improvement.

Manage and monitor clinical trial sites to ensure human subject protection, GCP and regulatory compliance. Conduct site visits (qualification, initiation, interim, close-out), track enrollment and study metrics, maintain study documents and TMFs, support start-up and safety activities, communicate with investigators and project teams, and provide training and reporting.

Senior Clinical Research Associate contractor responsible for overseeing clinical research activities, monitoring study conduct and compliance with protocols and regulations, managing documentation, and liaising with sponsors and cross-functional teams to support MedTech product development.

The Senior Clinical Research Associate coordinates clinical site monitoring, ensures compliance with regulations, and manages clinical trial documentation, training, and site relations.