About this role
Role Overview
- 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 study participants
- Responsible for managing and recording all phases of study protocol as required by the sponsoring agency
- Provides updates, understands study protocols, and collects patient data and information
- Performs clinical tasks including ECGs, collecting blood samples, and setting patients up with Holter monitors
- Active in recruiting study patients, managing study data collection, and performing clinical tasks related to the study
Requirements
- Bachelor’s degree or combination of education and/or experience may substitute for minimum education
- Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements)
- No specific work experience is required for this position
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)
- Tuition coverage for employees and their families