Clinical Research Coordinator I Non-RN Oncology FT Days

Company: AdventHealth Orlando
Location: Orlando
Posted on: November 22, 2021

Job Description:

DescriptionClinical Research Coordinator I Non-RN Oncology- AdventHealth Orlando -- Location Address:----601 EAST ROLLINS STREET, Orlando, 32803 Top Reasons to work at AdventHealth Orlando--

• Located on a lush tropical campus, our flagship hospital, 1,368-bed AdventHealth Orlando
• Our 40-bed Cardiopulmonary PCU--unit provides great opportunities to learn and grow with a caring specialized trained team. This unit cares for patients with cardiac and pulmonary needs such as pre/post heart catheterizations, pacemaker insertions, ablations, lead revisions, tikosyn and sotalol initiation, rapid atrial fibrillations, etc.
• 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
• Immediate Benefits
• Training opportunities--for--experienced--Registered Nurses that are either looking to grow into a higher acuity level or working outside of the hospital setting that are interested in transitioning to--acute care such as our Cardiopulmonary PCU unit. Work Hours/Shift:------FT/Days PRINCIPAL DUTIES AND JOB RESPONSIBILITIES: --- 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. --- Responsible for all aspects of research conducted including patient screening, assessing eligibility, and coordinating the participation 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 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. QualificationsKNOWLEDGE 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 --- Bilingual (English/Spanish) EDUCATION AND EXPERIENCE REQUIRED: --- Bachelor---s degree in Healthcare Administration, Research, or related field with no experience or --- Associates degree in Healthcare Administration, Research, or related field and two (2) years--- experience or --- Graduate of an accredited allied health certificate program with four (4) years of clinical research or healthcare experience. EDUCATION AND EXPERIENCE PREFERRED: --- Master---s degree in Healthcare Administration, Research, or related field LICENSURE, CERTIFICATION OR REGISTRATION REQUIRED: --- None 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)) --- BLS --- 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.

Keywords: AdventHealth Orlando, Orlando , Clinical Research Coordinator I Non-RN Oncology FT Days, Healthcare , Orlando, Florida