Clinical Research Coordinator – Entry Level

University of South Florida; Tampa (FL); On-site; USD 52,000 - 76,000; Full time

Job summary

University of South Florida is seeking a Clinical Research Coordinator I to coordinate screening, enrollment, and retention for clinical studies at the Tampa campus. The role involves direct patient assessments, data collection, and collaboration with the study team under lead coordinators and principal investigators.

Responsibilities include coordinating visits, assisting with site monitoring, ensuring regulatory compliance (HIPAA), and maintaining study documentation and vendor communications.

Qualifications

• Bachelor's degree in a related field or equivalent combination of education and experience.
• SB 1310 requirements may apply to eligibility for employment.

Responsibilities

• Coordinate and oversee screening, enrollment, and retention of study participants.
• Perform patient clinical assessments for trial visits including scheduling with vendors and other departments.
• Conduct study visits and data collection throughout the research study.
• Assist with implementation of procedures and activities of assigned study protocols.
• Communicate with the study team and clinical team on site protocols.
• Prepare and submit site study documents and assist with monitoring visits, audits, and inspections.
• Maintain site inventory and coordinate with vendors for research materials.
• Monitor compliance with the protocol, site SOPs, and HIPAA regulations.

Skills

Bachelor's degree in related field

SB1310 employment requirements

HIPAA compliance knowledge

Education

Bachelor's degree or equivalent

Job description

University of South Florida is seeking a Clinical Research Coordinator I to coordinate screening, enrollment, and retention for clinical studies at the Tampa campus. The role involves direct patient assessments, data collection, and collaboration with the study team under lead coordinators and principal investigators.

Responsibilities include coordinating visits, assisting with site monitoring, ensuring regulatory compliance (HIPAA), and maintaining study documentation and vendor communications.