Onsite Clinical Research Coordinator I - Data-Driven Trials

University of South Florida; Tampa (FL); On-site; USD 52,000 - 70,000; Full time

Job summary

University of South Florida seeks a Clinical Research Coordinator I to oversee screening, enrollment, and retention of study participants. The role supports data quality across projects under lead coordinators and principal investigators in a hospital research setting.

Responsibilities include IRB documentation, EPIC data extraction, tissue sample handling, and collaboration with physicians and nurses. This is an on-site position; visa sponsorship is not available.

Qualifications

• Bachelor's degree in a related field or equivalent combination of education and experience.
• SB 1310 guidance for public employers and education substitutions may apply.
• Experience with IRB processes and regulatory documentation.
• Understanding of clinical data management and patient privacy requirements.

Responsibilities

• Coordinate screening, enrollment, and retention of study participants.
• Prepare IRB submissions, regulatory documents, and sample handling procedures.
• Extract and curate clinical data from EPIC for study participants.
• Collaborate with researchers to prepare reagents and manage storage.
• Coordinate doctor notes and patient communications; convey guidance to patients.
• Maintain HIPAA-compliant REDCap database and ensure data integrity.
• Lead data analysis and reporting using MATLAB, RStudio, and Excel.

Skills

Data management

IRB coordination

Clinical research coordination

Communication

Attention to detail

Education

Bachelor's degree in related field

Tools

EPIC

REDCap

Excel

Tableau

MATLAB

RStudio

eCW

OnCore

Job description

University of South Florida seeks a Clinical Research Coordinator I to oversee screening, enrollment, and retention of study participants. The role supports data quality across projects under lead coordinators and principal investigators in a hospital research setting.

Responsibilities include IRB documentation, EPIC data extraction, tissue sample handling, and collaboration with physicians and nurses. This is an on-site position; visa sponsorship is not available.