The Clinical Research Coordinator in the Department of Neurology works with multidisciplinary teams to coordinate all aspects of clinical trial activities within the Neuromuscular Disease Program.
Requirements
- Recruit, evaluate, and educate participants and/or caregivers regarding clinical trials related to neuromuscular disease
- Conduct informed consent interviews with participants and caregivers
- Document trial-related activities in a timely and accurate manner
- Coordinate all aspects of study visit activities for participants and caregivers
- Collect and verify accurate medical history and concomitant medication information
- Monitor participants for any changes in health status
- Assist physicians with cerebrospinal fluid (CSF) collection for clinical trials
- Prepare and submit adverse event reports
- Maintain study documentation, including participant research records
- Ensure study staff complete required protocol training
Benefits
- Comprehensive Benefits Package
- Paid time off
- Generous employer contributions for health expense accounts
- Paid life insurance
- Long-term disability insurance
- Paid holidays
- Paid discretionary day
- Paid time off for bereavement, jury duty, military service, and parental leave
- Retirement program with generous employer contribution
- Additional voluntary retirement programs