Clinical Research Coordinator I RN

AdventHealth • Orlando, FL

120d

About The Position

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.

Requirements

• Associate degree in Nursing
• Current, active State of Florida license as a Registered Nurse
• BLS

Nice To Haves

• Bachelor's degree in Nursing
• 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)

Responsibilities

• Execute and coordinate the informed consent process for AdventHealth Research Institute participants in clinical trials and research studies across multiple locations.
• Deliver safe care and demonstrate regard for the dignity and respect of all participants.
• Maintain adequate skills in clinical competencies including but not limited to physical assessment, phlebotomy and IV insertion.
• Practice the principles of Universal Precautions and understand and abide by HIPAA regulations.
• Maintain a clean, prepared clinical space and perform set-up and turnover procedures in all clinical areas, per SOPs, in a timely manner.
• Participate in internal and/or external training programs to maintain licensure.
• Coordinate research participant recruitment and consenting for the therapeutic areas they serve.
• Provide 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.
• Collaborate with Clinical Research nursing staff, Research Services, laboratory teams, hospital departments, and physician offices to ensure ongoing regulatory and protocol compliance.
• Ensure compliant data entry/data mining into registries, patient records, and research specific database systems.
• Assist Principal Investigators and research staff in the development of compliant research protocols and other control documents.
• Serve 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.
• Maintain sensitivity to cost containment measures by conserving hospital supplies, equipment, and human resources while overseeing proposed project budgets.

Benefits

• Benefits from Day One
• Paid Days Off from Day One
• Career Development
• Whole Person Wellbeing Resources
• Mental Health Resources and Support
• Pet Insurance

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Ambulatory Health Care Services
• Education Level: Associate degree
• Number of Employees: 501-1,000 employees