Temporary Clinical Research Coordinator

📋 Description

• Support study startup activities, including development and maintenance of study workflows
• Assist with the configuration, testing, and operational readiness of study systems, including
• Support participant recruitment, prescreening, scheduling, informed consent coordination
• Review study documentation for completeness and follow up on missing, inconsistent, or incomplete
• Support the resolution of data queries, documentation discrepancies, and outstanding study action
• Maintain participant enrollment logs, screening logs, visit trackers, delegation logs, training

🎯 Requirements

• Bachelor's degree in life sciences, public health, psychology, nursing, clinical research, or a
• 2+ years of experience supporting clinical research, healthcare research, academic research, or
• At least 1 year of experience performing clinical research coordination, participant-facing
• Working knowledge of Good Clinical Practice and applicable human-subject research requirements.
• Strong organizational and time-management skills, with the ability to manage multiple participants
• Strong attention to detail and commitment to accurate, complete, and timely documentation.