Full-time · On-site
Clinical Research Coordinator III - Emergency Medicine
This is a high-level clinical research role focused on the fast-paced world of Emergency Medicine at a major university campus. It combines hands-on patient interaction with rigorous regulatory oversight, making it a perfect fit for a seasoned coordinator looking to manage complex, multi-faceted trials. The role is distinguished by its breadth, covering everything from phlebotomy to high-level grant reporting.
University of Florida · Jacksonville, Florida, United States · Posted 21 April 2026
The role
Overview
This is a high-level clinical research role focused on the fast-paced world of Emergency Medicine at a major university campus. It combines hands-on patient interaction with rigorous regulatory oversight, making it a perfect fit for a seasoned coordinator looking to manage complex, multi-faceted trials. The role is distinguished by its breadth, covering everything from phlebotomy to high-level grant reporting.
What they need
Requirements & Skills
Key Responsibilities
- Screen and enroll participants into IRB-approved clinical studies within the Emergency Department
- Conduct clinical follow-up visits including diagnostic testing and device education
- Maintain comprehensive regulatory binders and ensure audit readiness for study monitors
- Coordinate with pharmacy and hospital staff to manage investigational products
- Act as the primary liaison between investigators, sponsors, and the IRB
Essential
- Bachelor’s degree in a relevant field and three years of professional experience, or an equivalent combination of education and work history
- Proven ability to manage federal, industry, and private foundation grant-funded programs
- Experience with IRB protocols and regulatory documentation management
- Ability to perform clinical tasks including phlebotomy and vital sign monitoring
- Proficiency in data entry and database development for case report forms
Preferred
- Experience specifically within an Emergency Medicine or acute care research setting
- Familiarity with EPIC electronic health record systems for participant tracking
- Advanced knowledge of investigational product handling and drug accountability
Key Skills
Clinical specimen collection (nasopharyngeal, saliva, blood)Laboratory processingRegulatory compliancePatient screening and enrollmentPsychometric survey administrationInterdisciplinary communicationGrant administration
Networking
People to Know
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Perks
Benefits & perks
- Opportunity to work at a premier Tier-1 research institution
- Involvement in diverse, high-impact medical studies (Sepsis, Opioids, Precision Medicine)
- Collaborative academic environment
- Professional development in clinical research administration
Next step
Apply now
Found via careers.insidehighered.com