Clinical Trials Nurse Coordinator

UF Health; Jacksonville (FL); On-site; USD 60,000 - 90,000; Full time

Job summary

UF Health Jacksonville is seeking a registered nurse to coordinate clinical research studies, ensuring high-quality nursing care for participants in trials and coordinating imaging protocols with modality supervisors.

The role involves recruiting and screening participants, data entry in Rave and DataTrak, regulatory submissions, and timely reporting of adverse events while maintaining FDA-compliant documents.

Qualifications

• 2 years nursing experience required.
• Up to 1 year experience entering data in Rave and DataTrak.
• Ability to perform EKGs, phlebotomy, spin blood, prepare specimens for shipping.
• RN license (NCLEX-RN) required at time of hire.
• BLS preferred at time of hire.

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.
• Assures that adverse events are reported in timely fashion.
• Maintain Regulatory documents as mandated by FDA regulations.
• Assist/prepare initial institutional review board (IRB) and regulatory document submissions. Appropriately submit documents to the IRB.
• Assist/prepare and submit documentation to institutional review board (initial review, renewals, revisions, AE, protocol deviations)
• Other duties as assigned

Skills

Nursing

Data entry

EKG

Phlebotomy

Specimen shipping

Education

Bachelor's in Nursing

Associates in Nursing

High School Diploma

Tools

Rave

DataTrak

Job description

UF Health Jacksonville is seeking a registered nurse to coordinate clinical research studies, ensuring high-quality nursing care for participants in trials and coordinating imaging protocols with modality supervisors.

The role involves recruiting and screening participants, data entry in Rave and DataTrak, regulatory submissions, and timely reporting of adverse events while maintaining FDA-compliant documents.