Nurse Consultant

UNC-Chapel Hill • Chapel Hill, NC

1d

About The Position

The purpose of this position is to facilitate the conduct of oncology clinical trials, including subject and data management, according to federal regulations, Good Clinical Practice, and local and institutional policies. These responsibilities relate to the mission of the UNC / LCCC Protocol Office by maintaining the quality of research and by addressing patient safety and regulatory compliance which impact research quality and safeguard institutional integrity. The primary responsibilities of this position include the informed consent process, eligibility and screening, toxicity assessment, patient management, conducting in-services for nurses staff in treating clinic; planning of patient recruitment methods; logistics of patient visits; logistics of obtaining and coordinating clinical samples; specimen collection as needed, enlistment of support of necessary ancillary departments; coordinating the ordering of the required supplies; preparation of study tubes, collecting source documentation; Data entry / management for assigned studies, working with Clinical Research Associates to facilitate data collection for CRFs (case report forms) and/or eCRFs for trials as assigned; prepare and participate in monitoring visits; facilitate pre-site meetings, site initiation meetings, and plan, organize and run protocol start-up meetings.

Responsibilities

• Facilitate the conduct of oncology clinical trials, including subject and data management
• Informed consent process
• Eligibility and screening
• Toxicity assessment
• Patient management
• Conducting in-services for nurses staff in treating clinic
• Planning of patient recruitment methods
• Logistics of patient visits
• Logistics of obtaining and coordinating clinical samples
• Specimen collection as needed
• Enlistment of support of necessary ancillary departments
• Coordinating the ordering of the required supplies
• Preparation of study tubes
• Collecting source documentation
• Data entry / management for assigned studies
• Working with Clinical Research Associates to facilitate data collection for CRFs (case report forms) and/or eCRFs for trials as assigned
• Prepare and participate in monitoring visits
• Facilitate pre-site meetings, site initiation meetings, and plan, organize and run protocol start-up meetings.

What This Job Offers

• Job Type: Full-time
• Education Level: No Education Listed