Clinical Research Assistant
$20 - $23 per hourUniversity of Florida
Clinical Research Assistant Job no: 541987
Work type: Staff Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Allied Health
Department: 27320508 - HA-UFHCI CRO SOLID TUMOR Classification Title:
Clinical Research Assistant
Classification Minimum Requirements:
High School Diploma and one year of appropriate experience; or an equivalent combination of education and experience.
Job Description: The UF Health Cancer Institute is the 72nd NCI designated cancer center and the only one at a public university in the State of Florida. As a matrix cancer center, we span all of the University of Florida's 16 colleges, pulling together a world-class, multi-disciplinary membership of over 350 faculty and 180 staff to address the challenges of the cancer burden faced by the population we serve as we work together to find a cure.
As a Clinical Research Assistant at the UF Health Cancer Institute (UFHCI), you will be responsible for collaborating with study coordinators and research staff, investigators, physicians, nurses, and other key personnel in the clinics, hospitals, and at the Cancer Institute to ensure compliance with protocol requirements and satisfactory care for patients enrolled on research protocols.
In your new role you will be responsible for the following:
About the City of Gainesville Home to the University of Florida, one of the nation's top public universities, Gainesville offers vibrant academic and healthcare communities alongside an affordable cost of living, no state income tax, and mild winters. Enjoy the outdoors with over 30 miles of bike trails, freshwater springs, and numerous water activities, plus easy access to beaches and world-class theme parks.
Gainesville combines historic charm with modern amenities, including a great school system, a lively downtown, and farmers' markets and craft breweries. Discover professional growth and quality of life in Gainesville-where community, innovation, and work-life balance meet!
For more information, check out: The Guide to Greater Gainesville and Explore Gainesville in 60 seconds Required Qualifications: High school diploma or equivalent and one year of relevant experience; or an equivalent combination of education and experience. Preferred: Knowledge/Experience:
Applicants must upload a copy of the following documents to be considered for this position:
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
Health Assessment Required:Yes Advertised: 10 Nov 2026 Eastern Standard Time
Applications close: 24 Nov 2026 Eastern Standard Time Whatsapp Facebook LinkedIn Email App
Work type: Staff Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Allied Health
Department: 27320508 - HA-UFHCI CRO SOLID TUMOR Classification Title:
Clinical Research Assistant
Classification Minimum Requirements:
High School Diploma and one year of appropriate experience; or an equivalent combination of education and experience.
Job Description: The UF Health Cancer Institute is the 72nd NCI designated cancer center and the only one at a public university in the State of Florida. As a matrix cancer center, we span all of the University of Florida's 16 colleges, pulling together a world-class, multi-disciplinary membership of over 350 faculty and 180 staff to address the challenges of the cancer burden faced by the population we serve as we work together to find a cure.
As a Clinical Research Assistant at the UF Health Cancer Institute (UFHCI), you will be responsible for collaborating with study coordinators and research staff, investigators, physicians, nurses, and other key personnel in the clinics, hospitals, and at the Cancer Institute to ensure compliance with protocol requirements and satisfactory care for patients enrolled on research protocols.
In your new role you will be responsible for the following:
- Transcribing protocol-required clinical data from medical records into case report forms, OnCore/Epic in accordance with protocol requirements and timelines.
- Coordinating research sample collection and ensuring proper labeling, processing, storage, and shipping in compliance with safety, quality, and regulatory guidelines.
- Facilitating regulatory compliance by assisting with audits, submitting required documents to the IRB, and tracking study approvals and subject data in the Clinical Trials Management System.
- Supporting the coordination of clinical trial participants, including preparing study materials, attending research meetings, and ensuring protocol-specific tests and procedures are completed.
About the City of Gainesville Home to the University of Florida, one of the nation's top public universities, Gainesville offers vibrant academic and healthcare communities alongside an affordable cost of living, no state income tax, and mild winters. Enjoy the outdoors with over 30 miles of bike trails, freshwater springs, and numerous water activities, plus easy access to beaches and world-class theme parks.
Gainesville combines historic charm with modern amenities, including a great school system, a lively downtown, and farmers' markets and craft breweries. Discover professional growth and quality of life in Gainesville-where community, innovation, and work-life balance meet!
For more information, check out: The Guide to Greater Gainesville and Explore Gainesville in 60 seconds Required Qualifications: High school diploma or equivalent and one year of relevant experience; or an equivalent combination of education and experience. Preferred: Knowledge/Experience:
- Experience supporting clinical research and/or oncology-related programs.
- Associate's Degree in Nursing and/or Basic Sciences.
- One year of relevant experience or training in research and/or oncology.
- Experience working with databases and/or patient data.
- Familiarity with laboratory processes, including the collection, processing, storage, and shipment of human samples.
- Resourceful team player who can also work independently with professionalism and discretion.
- Strong emotional intelligence and ability to navigate complex situations collaboratively.
- Demonstrated ability to manage multiple priorities while interacting professionally with diverse stakeholders.
- Proficiency with Microsoft Office applications.
- Demonstrated ability to manage data accurately and maintain compliance with research protocols.
- Effective writing, organizational, and time management skills with strong attention to detail.
Applicants must upload a copy of the following documents to be considered for this position:
- Cover Letter or Letter of Interest
- Curriculum Vitae or Resume
- List of Three Professional References
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
Health Assessment Required:Yes Advertised: 10 Nov 2026 Eastern Standard Time
Applications close: 24 Nov 2026 Eastern Standard Time Whatsapp Facebook LinkedIn Email App
Vacancy posted 1 day ago
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