Clinical Research Coordinator II RN Tri Research

Adventist Health • Orlando, FL

135d

About The Position

The Clinical Research Coordinator II RN (CRC-II RN) serves the AdventHealth Research Institute (AHRI), under limited supervision, to plan, coordinate, evaluate and perform the nursing care of participants and collect data for assigned research projects. The CRC-II RN follows study specific protocol guidelines, communicates with AHRI Principal Investigators (PI), Sub-Investigators (Sub-I), Clinical Research Lead and clinical research support staff. The CRC-II RN works to advocate for the patient, while adhering to the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, Food and Drug Administration (FDA) regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) guidelines.

Requirements

• Associate degree in Nursing
• Minimum 2 years of Clinical Research experience
• Current, active State of Florida license as a Registered Nurse
• BLS

Nice To Haves

• Bachelor’s degree in Nursing
• Experience in area of specialty, as assigned
• Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA))
• Advanced Cardiovascular Life Support (ACLS)
• Other certification as applicable to clinical degree or program (i.e. medical assistant, medical technician, phlebotomy)

Responsibilities

• Delivers safe care and demonstrates regard for the dignity and respect of all participants.
• Maintains adequate skills in clinical competencies including but not limited to physical assessment, phlebotomy and IV insertion.
• Practices the principles of Universal Precautions.
• Understands and abides by HIPAA regulations.
• Maintains a clean, prepared clinical space.
• Participates in internal and/or external training programs to maintain licensure.
• Utilizes positive interpersonal communication skills; communicates effectively with members of the healthcare team, patients, investigators, sponsors of research and administration.
• Reviews all elements of the current institutional IRB approved informed consent (IC) document with study candidates and/or legal representative.
• Manages multiple clinical trial protocols, coordinates the execution and follow-up of each protocol.
• Performs accurate, legible and timely documentation.
• Manages records, study medication and test articles in a confidential and secure manner.
• Promotes Principal Investigator (PI) oversight by advising the PI, sub-investigator(s), Supervisor and/or Clinical Operations Manager of deviations in conduct, patient status, issues relevant to the integrity of the trial and/or the safety of research subjects.
• Coordinates the work of support staff, laboratory technicians, and assistants to ensure efficient, timely, and high-quality results and adherence to research protocols.
• Serves as liaison between Principal Investigators and the Institutional Review Board (IRB) and the Office of Sponsored Programs (OSP).
• Prepares and/or reviews all required documentation for clinical research study start up, execution, modification, renewal, and termination.

Benefits

• Benefits from Day One
• Paid Days Off from Day One
• Student Loan Repayment Program
• Career Development
• Whole Person Wellbeing Resources
• Mental Health Resources and Support
• Pet Insurance
• Debt-free Education (Certifications and Degrees without out-of-pocket tuition expense)
• Nursing Clinical Ladder Program

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree
• Number of Employees: 501-1,000 employees