Clinical Research Core Nurse

UNC-Chapel Hill • Chapel Hill, NC

9d • Onsite

About The Position

Position Summary NOTE : This position is located in Kannapolis, NC, appx. 2 hours from UNC’s main campus. The Clinical Research Core ( CRC ) provides human nutrition research investigators with multidisciplinary services and equipment in one location complete with examination rooms and equipment, pharmacy, phlebotomy laboratory, specimen laboratory, and furnished consultation rooms. This centralized facility provides investigators with a coordinated, quality-controlled, and quality-assured facility for the procurement, processing, storage, analysis and distribution of biologic specimens for basic, translational, and clinical research studies. Additionally, the CRC offers a metabolic kitchen specifically designed to support nutrition research as well as state-of-the-art resources for investigators through human metabolism and body composition assessments, clinical laboratory services, and preparation and delivery of precisely designed meals for study participants. Working under the general supervision of the CRC Manager, the CRC Nurse plays a critical role in supporting the research operation of the CRC and any clinical studies that utilize the services provided by the core. This position performs specialized medical procedures including IV management; operates specialized research equipment such as metabolic cart systems, Fibroscan devices, DXA systems, and Tanita body composition scales; and ensures accurate data collection and specimen processing. This position is expected to use considerable judgement and anticipate participant needs, especially when performing specialized procedures. This position is also responsible for the procurement, preparation, and distribution of biospecimens (blood, urine, saliva, and other specimens) following policies and procedures for collection, storage, processing, distribution, and quality control as set up by the CRC . Communication with principal investigators is also needed to ensure that biospecimens are collected according to specific criteria of a research study. This position will be responsible for ensuring informed consent was obtained, required registrations are in place, and the procurement and processing of samples follows HIPAA and established policies associated with responsible procurement and handling of human specimens. The CRC Nurse communicates with study participants for purposes of recruitment, retention, and scheduling. This role also involves collecting study measurements and providing instructions to study participants. This position assists with other study activities to ensure the successful completion of the study aims. Specific duties will vary depending on the needs of the study and may be subject to change over the course of the study. Our goal is to work together as a cohesive team to achieve research aims. Additional benefits associated with this position include the opportunity to join a research team that highly values professional development. We will work with the selected candidate to help build the skills and experiences desired to further their individual career goals. Due to the requirements of this position, we anticipate work will be completed on site in Kannapolis, NC. Work Schedule Typically, work hours will be approximately 7:30am-3:00pm Monday-Thursday with potential for early morning, evening, and some Saturday hours (weekends occasionally) to be shared across team members.

Responsibilities

• Performs specialized medical procedures including IV management
• Operates specialized research equipment such as metabolic cart systems, Fibroscan devices, DXA systems, and Tanita body composition scales
• Ensures accurate data collection and specimen processing
• Procurement, preparation, and distribution of biospecimens (blood, urine, saliva, and other specimens) following policies and procedures for collection, storage, processing, distribution, and quality control as set up by the CRC
• Communication with principal investigators is also needed to ensure that biospecimens are collected according to specific criteria of a research study
• Ensuring informed consent was obtained, required registrations are in place, and the procurement and processing of samples follows HIPAA and established policies associated with responsible procurement and handling of human specimens
• Communicates with study participants for purposes of recruitment, retention, and scheduling
• Collecting study measurements and providing instructions to study participants
• Assists with other study activities to ensure the successful completion of the study aims

Benefits

• opportunity to join a research team that highly values professional development
• We will work with the selected candidate to help build the skills and experiences desired to further their individual career goals

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed
• Number of Employees: 11-50 employees