Massachusetts Licensed Clinical Research Associate

Job Summary

Managing clinical monitoring activities for domestic and international studies, the full-time Massachusetts Licensed Clinical Research Associate will oversee study startup, conduct monitoring visits, and mentor team members while working remotely.

Key responsibilities

• Manage study startup activities including site selection, qualification visits, and activation
• Conduct regular monitoring visits to ensure compliance with study protocols and regulations
• Lead study closeout and database lock activities while serving as the primary contact for protocol compliance questions

Required qualifications

• B.S. or B.A. and/or an equivalent combination of education or experience
• CRA certification
• Minimum of 5 years of monitoring experience in clinical research
• Ability to travel on short notice and manage travel schedules independently
• Direct experience in executing clinical research studies