Entry-Level Clinical Research Assistant, Oncology Trials

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

Job summary

The University of Florida invites applications for an entry-level Clinical Research Assistant at UF Health Cancer Institute in Gainesville. You will collaborate with study coordinators, investigators, nurses, and staff to ensure protocol compliance and quality care for participants in cancer research protocols.

Responsibilities include transcribing data into CRFs (OnCore/Epic), coordinating sample collection, supporting IRB submissions and trial approvals, and assisting with participant

Qualifications

• Associate’s degree and/or relevant coursework in clinical research or oncology.
• Experience or training in research and/or oncology.
• Experience working with databases and/or patient data.
• Familiarity with laboratory processes including collection, processing, storage, and shipment of human samples.

Responsibilities

• Transcribing protocol data from medical records into case report forms (OnCore/Epic) per protocol and timelines.
• Coordinating research sample collection, labeling, processing, storage, and shipping per safety, quality, and regulatory guidelines.
• Assisting with audits and IRB submissions, tracking study approvals and subject data in the Clinical Trials Management System.
• Supporting coordination of clinical trial participants, including preparing study materials and attending research meetings.

Skills

Microsoft Office

Data management

Attention to detail

Time management

Education

Associate’s Degree in Nursing

Basic Sciences

Tools

OnCore

Epic

Job description

The University of Florida invites applications for an entry-level Clinical Research Assistant at UF Health Cancer Institute in Gainesville. You will collaborate with study coordinators, investigators, nurses, and staff to ensure protocol compliance and quality care for participants in cancer research protocols.

Responsibilities include transcribing data into CRFs (OnCore/Epic), coordinating sample collection, supporting IRB submissions and trial approvals, and assisting with participant