Clinical Research Coordinator II: Patient-Centric Trials

University of Florida; Jacksonville (FL); On-site; USD 55,000 - 65,000; Full time

Job summary

The Clinical Research Office (CRO) in the Office of Research Affairs (ORA), Dean’s Administration, College of Medicine‑Jacksonville is seeking a Clinical Research Coordinator II to coordinate, engage and perform research and regulatory functions for clinical studies.

This role involves screening and consenting patients, conducting study visits, and performing procedures such as vital signs, phlebotomy, and drug accountability, across multiple disciplines at UF facilities.

Qualifications

• Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.
• Valid driver’s license.

Responsibilities

• Coordinate, screen and consent patients across clinics and conduct research visits per protocols.
• Assist in regulatory submissions and prepare protocol/consent documents for IRB approval.
• Conduct prescreening, consenting and enrollment of participants and perform study visits and required procedures.
• Support investigators with proposal development, progress reports, budget creation and study files.

Skills

Communication skills

Data management

HIPAA knowledge

Phlebotomy

Education

Bachelor's degree in relevant area

Master's degree or allied health degree

Job description

The Clinical Research Office (CRO) in the Office of Research Affairs (ORA), Dean’s Administration, College of Medicine‑Jacksonville is seeking a Clinical Research Coordinator II to coordinate, engage and perform research and regulatory functions for clinical studies.

This role involves screening and consenting patients, conducting study visits, and performing procedures such as vital signs, phlebotomy, and drug accountability, across multiple disciplines at UF facilities.