Clinical Research Registered Nurse

Flourish Research•Jacksonville, FL

28d•Onsite

About The Position

Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. We are actively hiring a Clinical Research RN at our Jacksonville (University) research site location. The Clinical Research RN is responsible for the ethical and accurate management of Investigational Product (IP) and supplies for clinical trials under the direction of the Principal Investigator. The Research Nurse will work with Pharmacy staff and perform clinical duties requiring analysis, sound judgement, and a high level of knowledge of study specific protocols. Shift: Monday - Friday, 7 AM - 4 PM – hours may vary Location: 4085 University Blvd. South Suite 1 Jacksonville, FL 32216 Compensation: Hourly rate based on experience

Requirements

Registered Nurse
At least 1 year of clinical experience
Pleasant, outgoing, and mature. Good communication and time management skills. Attention to detail. Self-disciplined and motivated. Diligent and persistent.
High level of integrity and accountability
Ability to function effectively and positively in a team environment
Must have the ability to establish and maintain good working rapport with study patients, physicians,investigators, referring physicians, research staff and clinic
Familiar with medical terminology

Nice To Haves

Research experience - preferred

Responsibilities

Maintain familiarity with FDA regulations for clinical research
Administratively and clinically manage IP for blinded and unblinded clinical trials
Adhere to company Standard Operating Procedures, Good Clinical Practice and study protocols
Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
Dispense study medication in a professional and accountable manner
Provide subjects with proper IP administration training for in-office and home dosing
Complete source documentation (Accountability logs, subject source documentation, etc.)
Manage IP temperatures to ensure they remain in range and report any temperature excursions accordingly
Ordering and managing IP and IP supplies
Ensure prompt reporting of events to sponsor and IRB
Assess participant’s condition and report any significant variations from baseline measurements to study coordinator and Investigator
Ensure the filing and maintenance of all regulatory documents and IP related documentation
Schedule and prepare for monitoring visits
Assist monitors with accountability of used and unused IP and documentation
Maintain communication with Principal Investigator, Sub Investigators, Study Coordinators, Assistants, sponsors and IRB
Must exhibit accurate, complete, legible and timely use of communication methods