Clinical Research Coordinator I

Schedule: Monday-Friday, 8:00 AM-5:00 PM

Purpose Statement/Position Summary: The Clinical Research Office team is responsible for recruiting, enrolling, and coordinating clinical research studies for the Heart Institute. The Clinical Research Coordinator I assists principal investigators or other study team members with research studies and assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects. Additional responsibilities include regulatory work, study coordination, patient interaction, and sometimes facilitating contracts and budgets.

Minimum Qualifications/Work Experience: 1+ year experience in clinical trial coordination or computerized databases.

Preferred Qualifications

• Contracts, budget, and invoicing experience.
• Regulatory experience.
  
  

Education/Licensure/Certifications: High School Diploma, GED, or equivalent required. Bachelor’s degree preferred in related scientific field preferred. Certified clinical research associate/coordinator preferred.