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LPN Clin Research Coordinator | Neurology Downtown | Days | F/T at UF Health

Jacksonville, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

11 Oct, 26

Salary

0.0

Posted On

13 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Research Coordination, Patient Recruitment, Clinical Trial Management, Data Entry, Regulatory Compliance, Patient Screening, Medication Dispensing, Quality Assurance, Case Report Forms, Protocol Implementation

Industry

Hospitals and Health Care

Description

Overview Job Duties Works under the supervision of the Research Manager. Responsible for all aspects of research coordination for research studies; Responsible for research specific quality nursing care for patients participating in clinical trials. Responsibilities Essential Functions • Plan, implement and monitor participant recruitment and retention procedures. Screen and interview study participants. • Interpret and implement protocol procedures and policy. • Screen and interview study participants. • Maintain case report forms, charts and documentation. • Collect and enter research data in electronic data capture, review lab and procedure results. • Dispense study medication and maintain records. • Maintain regulatory compliance and documents as mandated by FDA regulations. • Open communication with study sponsors, Institutional Review Boards, and Research Office. • Assist study monitors and sponsors with site visits. • Assist audit services with internal study audits and reports. • Completes quality assurance assignments. • Arranges for study-related inpatient hospital services and assures that study related laboratory tests and diagnostic procedures are completed. Qualifications Experience Requirements 2 years LPN in ambulatory Setting required Education Requirements High School Diploma or GED required LPN License required Basic Life Support (BLS) required UFJPI is an Equal Opportunity Employer and Drug Free Workplace

Responsibilities

The coordinator manages all aspects of research studies, including participant recruitment, retention, and the implementation of protocol procedures. They are also responsible for providing quality nursing care to clinical trial participants and maintaining regulatory documentation.