• Monitor clinical trials and take notes on activities
• Ensure compliance with all clinical trial protocols
• Enter clinical research data into appropriate fields
• Transfer data from paper formats via computer, recorders, or scanners
• Organize spreadsheets with large numbers
• Curate data directly from clinical research
• Oversee clinical site activities
• Prepare correspondence, documentation, or presentation materials
• Draft informed consents for trials
• Audit research trials

Requirements and Qualifications

• Bachelor’s degree in a science or health related field
• Prior experience handling research responsibilities is a plus
• Proficient computer skills, including Microsoft Office Suite
• Self-directed and able to work without supervision
• Excellent written and verbal communication skills
• Ability to multitask, prioritize, and manage time efficiently

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