Site Research Assistant - Kansas City, MO

Requirements

• EDC data entry and query resolution
• Review patient charts and database records
• Build and maintain effective working relationships with investigators, clinical staff, and study teams
• Assist with screening, prescreening referrals, recruiting, and enrolling study participants
• Manage participant visit scheduling, reminders, and protocol-related logistical tasks
• Collect participant history and coordinate laboratory requirements and follow-up care
• Support the informed consent process, ensuring adherence to IRB-approved procedures
• Promote participant safety by following protocol guidelines and reporting requirements
• Ensure compliance with sponsor and company SOPs, policies, and regulatory expectations
• Maintain study supplies and assist with regulatory binder organization
• Record vital signs as required by protocol

Benefits

• 401k Matching