Job Duties
- Manage daily operations for assigned clinical trial projects
- Perform study procedures in accordance with GCP and study protocols
- Organize and maintain paper and electronic study data in a complete and correct manner
- Cultivate enthusiastic and professional relationships with patients and sponsors alike
- Work closely with recruitment and prescreening teams to meet study enrollment goals
- Conduct diagnostic, efficacy, and safety assessments as needed
Job Requirements
- Two (2) or more years of clinical research coordinator experience
- Attention to detail and the ability to handle multiple tasks with precision
- Demonstrated ability to work accurately and quickly with CTMS
- A command of professional spoken and written English