Clinical Research Assistant: Data Entry & Participant Support

University of South Florida; Tampa (FL); On-site; USD 42,000 - 62,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Life insurance

Tuition programs

Paid leave

Employee discounts

Job summary

University of South Florida is seeking a Clinical Research Assistant to support clinical research activities, including participant recruitment, data entry, and documentation. This entry-level role typically reports to the PI or Clinical Research Manager, with moderate supervision and adherence to study protocols.

Responsibilities include assisting with screening and enrollment, collecting vitals, coordinating visits, and ensuring accurate study documentation.

Qualifications

• High School Diploma or equivalent required.
• SB 1310: Post-secondary education requirements or substitution of work experience may apply.
• Public employer policy allows postsecondary degree as alternative to experience, within limits.
• Direct experience requirements may not be substituted for licensure or registration.
• Equivalence rules under SB 1310 for higher degrees apply to experience requirements.

Responsibilities

• Assist with evaluation of potential research participants.
• Assist with screening, enrollment, and retainment of participants at the site.
• Schedule participant visits and maintain records.
• Record data for each study participant per protocol.
• Coordinate and conduct site monitoring visits, audits, and inspections.

Skills

Basic computer skills

Education

High School Diploma or equivalent

Job description

University of South Florida is seeking a Clinical Research Assistant to support clinical research activities, including participant recruitment, data entry, and documentation. This entry-level role typically reports to the PI or Clinical Research Manager, with moderate supervision and adherence to study protocols.

Responsibilities include assisting with screening and enrollment, collecting vitals, coordinating visits, and ensuring accurate study documentation.