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AdventHealth

Clinical Research Coordinator II RN Oncology

AdventHealth, Orlando, Florida, us, 32885

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Clinical Research Coordinator II RN Oncology Join to apply for the

Clinical Research Coordinator II RN Oncology

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AdventHealth

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.

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

Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance

Paid Time Off from Day One

403-B Retirement Plan

4 Weeks 100% Paid Parental Leave

Career Development

Whole Person Well‑being Resources

Mental Health Resources and Support

Pet Benefits

Schedule

Full time

Shift

Day (United States of America)

Address

601 E ROLLINS ST, ORLANDO, Florida 32803

Job Description

Delivers safe care and demonstrates regard for the dignity and respect of all participants.

Maintains clinical competencies including physical assessment, phlebotomy, and IV insertion.

Practices the principles of Universal Precautions and understands HIPAA regulations.

Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice.

Ability to work independently in a fast‑paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner. Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures. Other duties as assigned. Collaborates with study sponsors and assists site monitors during visits. Serves as liaison between Principal Investigators, the Institutional Review Board, and the Office of Sponsored Programs. Coordinates the work of support staff, laboratory technicians, and assistants to ensure efficient and high‑quality results. Promotes Principal Investigator oversight by advising on deviations, patient status, and trial integrity. Manages multiple clinical trial protocols, coordinates execution and follow‑up, and performs accurate documentation. Reviews informed consent documents with study candidates and ensures patient advocacy and safety. Maintains a clean and prepared clinical space, performing set‑up and turnover procedures as needed. Participates in internal and external training programs to maintain licensure. Utilizes positive interpersonal communication skills with healthcare team members, patients, investigators, sponsors, and administration. Works flexible hours and is available for research project‑related questions.

Qualification Requirements

Associate's of Nursing (Required), Bachelor's of Nursing, Advanced Cardiac Life Support Cert (ACLS) - RQI Resuscitation Quality Improvement, Basic Life Support - CPR Cert (BLS) - RQI Resuscitation Quality Improvement, Certified Clinical Research Coordinator (CCRC) - EV Accredited Issuing Body, Certified Clinical Research Professional (SOCRA) (CCRP) - EV Accredited Issuing Body, Oncology Certified Nurse (OCN) - EV Accredited Issuing Body, Registered Nurse (RN) - EV Accredited Issuing Body

Pay Range

$65,582.40 - $108,646.85

This facility is an equal opportunity employer and complies with federal, state and local anti‑discrimination laws, regulations and ordinances.

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