Site Educator

Perform clinical procedures to collect, record, and report data on patients enrolled in clinical studies. Assist with daily workload planning and provide clinical research support to investigators.

Requirements

• Review study protocols, Case Report Forms, and electronic data capture systems
• Attend all relevant study meetings and review meetings for Site Requirements
• Good command of English, French, or Arabic
• Good knowledge of clinical research and Good clinical practice certification
• Collect and submit regulatory/ethics documentation
• Assess site to be in line with GCP
• Orient research subjects to the study
• Maintain adherence to investigator site staff training requirements
• Prepare for and attend study monitoring visits, study audits, and regulatory inspections