This position assists investigators as coordinator of a basic to moderately complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance. This position works directly in the emergency department recruiting and enrolling patients into clinical trials.
Requirements
- Implements and manages all phases of study/protocol
- Ensures compliance with protocol guidelines and requirements of regulatory agencies
- Recruits and enrolls study participants
- Makes determinations of participants’ progress in the study
- Analyzes, investigates and reports adverse events
- Makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants
- Resolves protocol management issues and recommends corrective action as appropriate
Benefits
- Up to 22 days of vacation
- 10 recognized holidays
- Sick time
- Competitive health insurance packages with priority appointments and lower copays/coinsurance
- Free Metro transit U-Pass for eligible employees
- Defined contribution (403(b)) Retirement Savings Plan
- Wellness challenges
- Annual health screenings
- Mental health resources
- Mindfulness programs and courses
- Employee assistance program (EAP)
- Financial resources
- Access to dietitians
- Four weeks of caregiver leave to bond with your new child
- Family care resources
- Tuition coverage for you and your family