Research Associate-Radiology-Full-Time-Days

UF Health; Manhattan Beach (FL); Sur place; USD 52 000 - 70 000; Plein temps

Avantages offerts par ce poste

Equal Opportunity Employer

Drug-free Workplace

Résumé du poste

UF Health is seeking a detail-oriented professional to assist in conducting and coordinating clinical trials, ensuring adherence to protocols, GCP, and departmental procedures under supervision.

The position involves screening participants, collecting data from multiple sources, maintaining study documentation, and supporting billing and scheduling tasks for study visits. A high school diploma is required, with Associates preferred.

Qualifications

• Assists with screening and consenting potential participants in research studies.
• Adheres to protocol-specific procedures and GCP guidelines.
• Performs quality checks on case report forms and related documents.
• Maintains billing records for study visits and tracks fees.

Responsabilités

• Collects data from patient charts, medical records, interviews and questionnaires.
• Tracks patient visits and coordinates scheduling with front desk.
• Completes and organizes Case Report Forms and submits documents.
• Provides support to coordinators in data management and regulatory compliance.

Connaissances

Regulatory knowledge

Clinical trial coordination

Data collection

Attention to detail

Formation

High School Diploma

Associates preferred

Description du poste

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