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Established in 1997 and now a 203-bed hospital, AdventHealth Celebration Health was designed as a Mediterranean resort-style facility to serve as a cornerstone of health in Disney’s planned community of Celebration, Florida
The hospital consistently delivers a state-of-the-art healing environment to residents of Osceola, Orange, Polk and Lake Counties, as well as to visitors from across the United States and the world. All within a 'living laboratory' of groundbreaking, research-driven clinical solutions that integrate mind, body and spirit in the defeat of illness and disease.
The Imaging department at AdventHealth Celebration Health is integrally involved across the spectrum of patient care, assisting medical staff in the diagnosis and treatment of patients ranging from routine imaging studies to advanced interventional procedures. Annually, Imaging at Celebration Health performs 132,000 procedures across emergency, inpatient, surgical, and outpatient settings. The department operates within the hospital and services the greater Osceola community. The Imaging team includes more than 100 skilled and engaged staff including Radiologists, Technologists, Nurses, and support staff, working to ensure the patients receive appropriate, quality procedures and results at the right time.
Full Time, M-F Days, 5/8’s
You Will Be Responsible For:
Execute and coordinate the informed consent process for AdventHealth Research Institute participants in clinical trials and research studies across multiple locations. This may require travel between sites and research laboratories, and/or the use of technology.
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.
Responsible for all aspects of research conducted including patient screening, assessing (clinical) eligibility, and coordinating the care and follow-up of volunteers placed on research studies, trials, and programs.
Coordinate research participant recruitment and consenting for the therapeutic areas they serve
Provision of concierge level service for all patient facing interactions during the course of clinical trials and research studies
Coordinate or perform biospecimen collection (i.e. blood, tissue) and maintain HIPAA protected database connecting patient information to biospecimens used in research; perform patient chart review and data collection.
Collaborative interaction with Clinical Research nursing staff, Research Services, laboratory teams, hospital departments, and physician offices, to ensure ongoing regulatory and protocol compliance.
Through collaboration with assistant clinical coordinators, ensures compliant data entry/data mining into registries, patient records, and research specific database systems.
Assists Principal Investigators and research staff in the development of compliant research protocols and other control documents.
Serves as the study-specific clinical point of contact for participants, investigators, research staff, hospital departments and external research partners.
Collaborate with clinical research supervisors and staff to implement standard operating procedures (SOP) for the Institutes research division intended to meet standards. Ensures all patient-facing activities are compliant with clinical research standards and AHRI procedures.
Maintain sensitivity to cost containment measures by conserving hospital supplies, equipment, and human resources while overseeing proposed project budgets from internal and external funding sources.
What Will You Need:
KNOWLEDGE AND SKILLS REQUIRED:
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
Ability to acclimate and integrate into various clinical settings as needed per protocol
Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures.
Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research
Ability to communicate effectively with research participants, investigators, research staff and external partners.
Ability to apply analytical approach to problem solving, obtain and analyze facts, and apply sound judgement.
Ability to accept direction and respond to the changing needs of clinical research units
Working knowledge of Microsoft Office applications, such as, Word, Excel, Access, Outlook, and Internet knowledge and skill
KNOWLEDGE AND SKILLS PREFERRED:
Specialized knowledge of the unique needs of patients in the assigned therapeutic areas undergoing treatment
Specialized knowledge of assigned therapeutic areas as it relates to research and clinical trials.
One to two years skill in human life sciences/biomedical research; physiological, cellular, biochemical, or molecular biology
EDUCATION AND EXPERIENCE REQUIRED:
Associate degree in Nursing
EDUCATION AND EXPERIENCE PREFERRED:
Bachelor’s degree in Nursing
LICENSURE, CERTIFICATION, OR REGISTRATION REQUIRED:
Current, active State of Florida license as a Registered Nurse
LICENSURE, CERTIFICATION, OR REGISTRATION PREFERRED:
Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA))
Other certification as applicable to clinical degree or program (i.e. medical assistant, medical technician, phlebotomy)
The Clinical Research Coordinator I (RN) is involved in all aspects of research conducted including patient screening, assessing eligibility, and coordinating the care and follow-up of volunteers placed on research studies, trials, and programs. Specific activities to include: Research participant recruitment and consenting for the therapeutic areas they serve, provision of concierge level service for all patient facing interactions during the course of clinical trials and research studies, and the coordination of biospecimen collection (i.e. blood, tissue) through collaborative interaction with Clinical Research nursing staff, laboratory teams, hospital departments to ensure ongoing regulatory and protocol compliance.
Through collaboration with research assistants and/or clinical coordinators, ensures compliant data entry/data mining into registries, patient records, and research specific database systems. Assists Principal Investigators and research staff in the development of compliant research protocols and other control documents. Serves as the study-specific clinical point of contact for participants, investigators, research staff, hospital departments and external research partners. Actively participates in outstanding customer service and accepts responsibility in maintaining relationships that are equally respectful to all.
AdventHealth Greater Orlando (formerly Florida Hospital) is one of the largest faith-based health care providers in the United States. For 150 years, we have carried on a tradition of providing whole-person care that not only addresses patients' physical ailments, but also supports their emotional and spiritual well-being. We demonstrate the same level of compassion and care for our employees as well, doing all that we can to help them realize their full potential – both personally and professionally.