Description
Haik Humble Eye Center is seeking a detail-oriented, thorough, and organized clinical research assistant to join our growing healthcare family. In this position, you will play a key role in monitoring clinical trials to ensure compliance with procedures and protocols. You will document your findings, assist in recording research from trials, and organize large amounts of data.
Duties and Responsibilities
- 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 on findings
- Draft informed consents for trials
- Audit research trials
Requirements
- Bachelor’s degree in a science, psychology, or related field or Ophthalmology experience
- 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
