Research Analyst

• Serve as a primary point of contact for research participants during clinic visits
• Review medical histories and collect participant information to support study screening and enrollment activities
• Facilitate and witness the informed consent process
• Perform protocol-required clinical procedures, including vital signs collection, height, weight, BMI measurements, specimen collection, and phlebotomy
• Accurately document participant data and maintain study records in accordance with study protocols and Good Clinical Practice (GCP) guidelines
• Explain study procedures and schedules to participants while addressing questions
• Assist clinical teams during dosing days, including participant preparation, monitoring, and study-related procedures
• Support participant safety through observation, communication, and escalation of concerns
• Collaborate with nurses, physicians, and study teams to ensure protocol compliance and efficient study execution
• Participate in evening and overnight clinical operations as required

Explore Part Time Medical Research Associate at ICON plc. Review requirements and application details.