Participant Screening: Perform phone screenings or prescreen participants for eligibility.
Medical Record Review: Conduct thorough reviews of patient medical records.
Scheduling: Arrange in-patient visits and follow-up appointments, and send reminders.
Requirements
emr
clinical trials
problem solving
detail
precision
1 year
This role operates during standard business hours in a dynamic, fast-paced research setting. It requires precision, adaptability, and a commitment to high-quality data management.
Strong attention to detail and problem-solving skills.
Proficiency with Electronic Medical Records (EMR) systems and clinical trial management tools.
Minimum of 1 year of experience in clinical research coordination.
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
Medical, dental & vision
Employee Assistance Program
Life Insurance (Voluntary Life & AD&D for the employee and dependents)