RN Clinic Research Coordinator | Proton/Cardiology Research Downtown | Days | Full Time

Job description

Overview
Job Duties
Responsible for all aspects of research coordination for research studies; Responsible for research specific quality nursing
care for patients participating in clinical trials. Work with modality supervisors for completion of site questionnaires,
implementation of imaging protocol and coordinate services for research patients.
Responsibilities
Essential Functions
• Plan, implement and monitor participant recruitment and retention procedures.
• Interpret and implement protocol procedures and policy.
• Screen and interview study participants. Review lab and procedure results.
• Maintain case report forms, charts and documentation.
• Review protocols from other departments that include radiology services and prepare detailed responses
• Dispense medication and maintain records.
• Assures that adverse events are reported in timely fashion.
• Maintain Regulatory documents as mandated by FDA regulations.
• Assist/prepare initial institutional review board (IRB0 and regulatory document submissions. Appropriately submit

documents to the IRB.
• Assist/prepare and submit documentation to institutional review board (initial review, renewals, revisions, AE, protocol deviations)
• Other duties as assigned

Qualifications
Experience Requirements
2 years Nursing required
Up to 1 year Experience in entering data onto systems such as Rave and DataTrak preferred
Up to 1 year Ability to perform EKGs, perform phlebotomy, spin blood, prepare specimens for shipping, and
have certification of transport of biological materials. preferred
Education Requirements
Bachelors Nursing preferred
Associates Nursing required
High School Diploma required
Certification/Licensure Requirement
Registered Nurse (RN) required at time of hire
Basic Life Support (BLS) preferred at time of hire
NCLEX-RN required
UFJPI is an Equal Opportunity Employer and Drug Free Workplace
Essential Functions
• Plan, implement and monitor participant recruitment and retention procedures.
• Interpret and implement protocol procedures and policy.
• Screen and interview study participants. Review lab and procedure results.
• Maintain case report forms, charts and documentation.
• Review protocols from other departments that include radiology services and prepare detailed responses
• Dispense medication and maintain records.
• Assures that adverse events are reported in timely fashion.
• Maintain Regulatory documents as mandated by FDA regulations.
• Assist/prepare initial institutional review board (IRB0 and regulatory document submissions. Appropriately submit

documents to the IRB.
• Assist/prepare and submit documentation to institutional review board (initial review, renewals, revisions, AE, protocol deviations)
• Other duties as assigned