RN Clinical Research Coordinator II

Texas Health Huguley FWS; Orlando (FL); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading healthcare organization in Florida seeks an RN Clinical Research Coordinator II to join their team at AdventHealth Orlando. This role requires supporting clinical research initiatives, ensuring the safety of participants, and coordinating research activities while adhering to regulatory standards. The ideal candidate will have a strong RN background with at least two years of clinical research experience. A Bachelor's degree in Nursing and additional certifications are preferred. This is a full-time position offering competitive benefits and the opportunity for professional development.

Benefits

Benefits from Day One

Paid Days Off from Day One

Mental Health Resources and Support

Pet Insurance

Debt-free Education

Qualifications

• Minimum 2 years of Clinical Research experience.
• Current, active State of Florida license as a Registered Nurse.
• BLS and preferred certifications such as Clinical Research Coordinator.

Responsibilities

• Plan, coordinate, and perform nursing care for research participants.
• Ensure compliance with clinical trial protocols and FDA regulations.
• Manage multiple clinical trial protocols and documentation.

Skills

Patient Advocacy

Clinical Competencies

Interpersonal Communication

Education

Bachelor’s degree in Nursing

Job description

Job Description - RN Clinical Research Coordinator II (24042835)

Job Description

RN Clinical Research Coordinator II (

Job Number:

24042835 )

Description

Clinical Research Coordinator II -RN – AdventHedalth Orlando

All the benefits and perks you need for you and your family:

- Benefits from Day One

- Paid Days Off from Day One

- Mental Health Resources and Support

- Pet Insurance*

- Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)

* Nursing or BU specific benefits and perks

Our promise to you:

Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.

Schedule: Full Time, Days

Shift : Monday- Friday 8am – 5pm

The community you’ll be caring for: AdventHealth Orlando

• Located on a lush tropical campus, our flagship hospital, 1,368-bed AdventHealth Orlando
• Serves as the major tertiary facility for much of the Southeast, the Caribbean and South America
• AdventHealth Orlando houses one of the largest Emergency Departments and largest cardiac catheterization labs in the country
• We are already one of the busiest hospitals in the nation, providing service excellence to more than 32,000 inpatients and 125,000 outpatients each year

The role you’ll contribute:

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.

The value you’ll bring to the team: 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.May perform set-up and turnover procedures in all clinical areas, per SOP’s, in a timely manner.

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, according to current FDA, state, federal and institutional regulations with study candidates and/or legal representative; ensures, through patient advocacy and informed consent as an ongoing process, that the rights, safety and well-being of trial subjects are the most important considerations and should prevail over the interests of science and society.(Add from Chart)

Manages multiple clinical trial protocols, coordinates the execution and follow-up of each protocol, seeks and utilizes resources and works independently; performs accurate, legible and timely documentation. Manages records, study medication and test articles in 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; abides by hospital and departmental policies and SOPs, as well as all applicable local, state, and federal regulations.

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 and will meet all reasonable deadlines for submission. Maintains timely turnaround of all documents to avoid delays in study initiation and/or progress. Remains current on rapidly changing regulatory requirements and HIPAA regulations and implements these changes as appropriate and in a timely manner.

Qualifications

The expertise and experiences you’ll need to succeed :

• Minimum 2 years of Clinical Research experience
• Current, active State of Florida license as a Registered Nurse
• BLS
• Preferred qualifications:
• 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)