Research Associate-Radiology-Full-Time-Days
UF Health
Jacksonville, FL · Posted June 18, 2026
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How AI is used in this kind of work
Among operations research analysts, AI is already used for a large share of the tasks. Measured exposure for operations research analysts: 43% (high).
Share of this job’s tasks that AI is already used for at work, from real usage. It is not a forecast of job loss, and a low number means no use seen yet. Source: Anthropic Economic Index.
About the job
Overview
Description :
Assist in the conduct and coordination of clinical trials by insuring compliance with clinical protocol requirements, institutional and federal guidelines and department procedures under the direct supervision of the manager.
Responsibilities
Job Requirement:
Assists with screening and consenting potential participants interested in research clinical studies.
Adheres to ongoing clinical trial protocol-specific procedures as well as good clinical practice and departmental standard operating procedures.
Performs quality assurance checks on Informed Consent Forms, Case Report Forms and other research related documents.
Assists Coordinators with maintaining monthly billing for study visits and documents appropriate fees on research referral forms.
Assists Coordinators with the collection of data from patient charts, medical records, interviews, questionnaires and other sources.
Tracks required patient visits and coordinators scheduling with front desk.
Completes, submits and organizes Case Report Forms.
Qualifications
Qualification
Experience Request:
2 years Experience in research regulatory experience strongly recommended preferred
Education :
High School Diploma required Associates preferred
Additional Duties:
Additional duties as assigned may vary.
UFJPI is an Equal Opportunity Employer and Drugfree Workplace
Job Requirement:
Assists with screening and consenting potential participants interested in research clinical studies.
Adheres to ongoing clinical trial protocol-specific procedures as well as good clinical practice and departmental standard operating procedures.
Performs quality assurance checks on Informed Consent Forms, Case Report Forms and other research related documents.
Assists Coordinators with maintaining monthly billing for study visits and documents appropriate fees on research referral forms.
Assists Coordinators with the collection of data from patient charts, medical records, interviews, questionnaires and other sources.
Tracks required patient visits and coordinators scheduling with front desk.
Completes, submits and organizes Case Report Forms.
Qualification
Experience Request:
2 years Experience in research regulatory experience strongly recommended preferred
Education :
High School Diploma required Associates preferred
Additional Duties:
Additional duties as assigned may vary.
UFJPI is an Equal Opportunity Employer and Drugfree Workplace