RN Clinical Research Coordinator II

AdventHealth; Orlando (FL); On-site; USD 55,000 - 80,000; Full time

Job summary

A leading healthcare organization in Orlando is seeking a Clinical Research Coordinator II RN to join their research team. In this role, you'll oversee the nursing care and data collection for clinical trials, ensuring compliance with regulations and enhancing patient safety. Candidates must have a nursing degree and clinical research experience. This is a full-time position with opportunities for professional growth and community involvement.

Benefits

Benefits from Day One

Paid Days Off from Day One

Career Development

Whole Person Wellbeing Resources

Mental Health Resources and Support

Pet Insurance

Debt-free Education

Qualifications

• Minimum 2 years of Clinical Research experience required.
• Current State of Florida license as a Registered Nurse needed.
• BLS certification is necessary.

Responsibilities

• Coordinate nursing care of participants for research projects.
• Ensure adherence to study protocols and regulatory requirements.
• Manage multiple clinical trial protocols while maintaining records.

Skills

Clinical Research

Patient Advocacy

Communication

Clinical Competencies

Education

Associate degree in Nursing

Bachelor’s degree in Nursing

Job 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

- 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_ _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_

**Location:** 2501 N Orange Ave, Orlando FL 32803

**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._

**The expertise and experiences you’ll need to succeed** **:**

+ **Minimum qualifications** :

+ Associate degree in Nursing

+ 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)

This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances. The salary range reflects the anticipated base pay range for this position. Individual compensation is determined based on skills, experience and other relevant factors within this pay range. The minimums and maximums for each position may vary based on geographical location.

**Category:** Research

**Organization:** AdventHealth Orlando

**Schedule:** Full-time

**Shift:** 1 - Day

**Req ID:** 24042835

We are an equal opportunity employer and do not tolerate discrimination based on race, color, creed, religion, national origin, sex, marital status, age or disability/handicap with respect to recruitment, selection, placement, promotion, wages, benefits and other terms and conditions of employment.