Clinical Research Coordinator: Cardiology Trials (RN)

University of Florida Jacksonville Physicians, Inc.; Jacksonville (FL); On-site; USD 65,000 - 85,000; Full time

Job summary

University of Florida Jacksonville Physicians, Inc. in Jacksonville, FL seeks a Research Coordinator with nursing credentials to manage clinical trial coordination, patient recruitment and regulatory documentation.

You will ensure protocol adherence, data integrity and participant safety throughout study conduct. The role requires maintaining study records, interfacing with IRB submissions and data management tasks, while ensuring compliance with FDA regulations and trial protocols.

Qualifications

• 2 years nursing experience required.
• Experience entering data into systems like Rave/DataTrak preferred.
• Ability to perform EKGs, phlebotomy, spin blood and shipping prep; transport of biological materials preferred.

Responsibilities

• Plan, implement and monitor participant recruitment and retention procedures.
• Interpret and implement protocol procedures and policy.
• Screen and interview study participants; review lab and procedure results.
• Maintain case report forms, charts and documentation.
• Review protocols from other departments that include radiology services and prepare detailed responses.
• Dispense medication and maintain records.
• Assure adverse events are reported in timely fashion.
• Maintain regulatory documents as mandated by FDA regulations.
• Assist/prepare initial IRB and regulatory submissions; submit documents to the IRB.
• Assist/prepare and submit documentation to IRB (initial review, renewals, revisions, AE, protocol deviations).
• Other duties as assigned

Skills

Nursing

Education

Bachelor's in Nursing preferred

Associates in Nursing required

High School Diploma required

Job description

University of Florida Jacksonville Physicians, Inc. in Jacksonville, FL seeks a Research Coordinator with nursing credentials to manage clinical trial coordination, patient recruitment and regulatory documentation.

You will ensure protocol adherence, data integrity and participant safety throughout study conduct. The role requires maintaining study records, interfacing with IRB submissions and data management tasks, while ensuring compliance with FDA regulations and trial protocols.