Obtains informed consent and supports enrollment into clinical trials.
Provides patient education regarding research study.
Interacts with consortium members, organizes meetings and communicates with participating institutions, tracks and records progress, schedules meetings, records and distributes minutes.
Collects and documents clinical information (data) from study participants.
Requirements
Benefits
Critical Illness, Accident, and Hospital
Time Off/Leave (PTO, Vacation or Sick Leave)
Short and long-term disability
401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
Health Spending Account (HSA)
Medical, dental & vision
Employee Assistance Program
Life Insurance (Voluntary Life & AD&D for the employee and dependents)