Pediatric Infectious Disease Research Coordinator II

University of Florida; Gainesville (FL); On-site; USD 59,000 - 67,000; Full time

Job summary

University of Florida seeks a Clinical Research Coordinator II for Pediatric ID at the Jacksonville Campus. You will independently coordinate treatment, observational and data-based studies, manage visits, consent, data collection, and regulatory compliance under GCP and sponsor requirements.

Responsibilities include participant recruitment and retention, study logistics, coordination with investigators, sponsors, and UF CARES staff, and ensuring accurate documentation in Epic; involvement in

Qualifications

• Bachelor's degree in an appropriate area and two years of relevant experience, or an equivalent combination.
• Experience coordinating HIV/AIDS or infectious disease studies preferred.
• Clinical Research Certification (CCRC/CCRP) preferred or obtainable within two years of hire.
• Excellent communication with investigators, sponsors, and participants.

Responsibilities

• Identify, recruit, and screen potential research participants per protocol.
• Coordinate informed consent/assent and maintain documentation in the research record and Epic.
• Plan and coordinate study visits, procedures, and data collection per protocol.
• Ensure regulatory compliance, adverse event reporting, and timely data queries.
• Perform protocol-required phlebotomy and specimen management as applicable.
• Communicate with investigators, sponsors, monitors, and UF CARES staff about study activities.

Skills

Clinical research coordination

Regulatory compliance

Data management

Education

Bachelor's degree in an appropriate area

Tools

Epic

Job description

University of Florida seeks a Clinical Research Coordinator II for Pediatric ID at the Jacksonville Campus. You will independently coordinate treatment, observational and data-based studies, manage visits, consent, data collection, and regulatory compliance under GCP and sponsor requirements.

Responsibilities include participant recruitment and retention, study logistics, coordination with investigators, sponsors, and UF CARES staff, and ensuring accurate documentation in Epic; involvement in