Clinical Research Assistant — Study Enrollment & Data Entry

Tampa General Hospital; Tampa (FL); On-site; USD 42,000 - 56,000; Full time

Job summary

Tampa General Hospital is seeking a Clinical Research Assistant to support multiple core research projects at the Core-Ctr For Research Excel. Responsibilities include pre-screening participants, obtaining informed consent, coordinating visits, and data entry into EDC/EMR systems.

You will review lab manuals, process specimens per protocol, and liaise with study teams while maintaining PHI privacy and regulatory compliance. This is an on-site role at the Tampa Main Campus.

Qualifications

• Bachelor's degree in a science or health-related field.
• Working knowledge of clinical research concepts, regulations, and GCP principles.
• Ability to interpret study protocols and apply inclusion/exclusion criteria during pre-screening.
• Understanding of informed consent requirements and ability to explain studies to participants.

Responsibilities

• Pre-screen potential participants against protocol eligibility.
• Obtain and document informed consent for registry/observational studies and minimal-risk device studies.
• Assist with subject enrollment, randomization, and coordination of research visits.
• Review study lab manuals and collect/process specimens per protocol.
• Perform accurate data entry from source documents to forms (paper/electronic).
• Serve as liaison between research staff and research sites.

Skills

Pre-screening criteria

EDC systems

EMR access

Data entry accuracy

PHI privacy

Communication

Team collaboration

Time management

Education

Bachelor's Degree - science/health related

Tools

EDC systems

EMR

Office software (Word/Excel/Outlook)

Job description

Tampa General Hospital is seeking a Clinical Research Assistant to support multiple core research projects at the Core-Ctr For Research Excel. Responsibilities include pre-screening participants, obtaining informed consent, coordinating visits, and data entry into EDC/EMR systems.

You will review lab manuals, process specimens per protocol, and liaise with study teams while maintaining PHI privacy and regulatory compliance. This is an on-site role at the Tampa Main Campus.