Research Associate-Radiology-Full-Time-Days

University of Florida Jacksonville Physicians, Inc.; Jacksonville (FL); On-site; USD 40,000 - 55,000; Full time

Job summary

The University of Florida Jacksonville Physicians, Inc. seeks a Clinical Research Coordinator to assist in conducting clinical trials. Responsibilities include screening participants, ensuring compliance with protocols, and performing quality assurance checks on research documents.

Ideal candidates will have at least 2 years of research regulatory experience and a minimum of a High School Diploma; an Associate's degree is preferred. This role supports coordinators in managing data collection and billing for study visits.

Qualifications

• At least 2 years of experience in research regulatory processes is strongly recommended or preferred.

Responsibilities

• Assist in screening and consenting potential participants for clinical trials.
• Ensure compliance with clinical protocol and guidelines.
• Perform quality assurance on research documentation.
• Support coordinators with billing and data collection.
• Track patient visits and coordinate schedules.

Education

High School Diploma

Associates Degree

Job description

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

• 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

• Experience: 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