NAMSA Benefits Overview

Manages clinical research studies involving site monitoring, human subject protection, GCP and regulatory compliance. Coordinates site qualification, initiation, interim and close-out visits; maintains study documents and metrics; supports audits, submissions, safety activities, data management, protocol development and trial registration. Serves as a liaison among investigative sites, clients and study teams, and provides training and mentoring to CRAs. Travel may range from 20% for in-house roles to 80% for field roles.

Manages clinical research studies involving site monitoring, human subject protection, GCP and regulatory compliance. Coordinates site qualification, initiation, interim and close-out visits; oversees study documentation, metrics, training, audits, budgets, safety activities and regulatory submissions. Supports protocol development, data management, core laboratory operations, literature reviews and trial registration. Mentors CRAs and communicates study performance, risks and progress to investigators, clients and internal teams.