Site Coordinator

Conduct assigned site study tasks, resolve queries, and assist with SAE notifications. Help the investigator with patient recruitment, schedule patient visits, and manage study drug accountability logs. Facilitate Ethics Committee submissions, update investigator files, and attend monitoring visits, audits, or inspections as required. Manage sample management and process patient expense payments. Assist in investigator meetings or training when needed. Maintain high organizational skills to prioritize competing priorities and adapt to changing timelines while ensuring study quality and milestone achievement.