Nurse Consultant

UNC-Chapel Hill•Chapel Hill, NC

3d•Onsite

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.

Requirements

Facilitate the conduct of oncology clinical trials.
Manage subject and data according to federal regulations, Good Clinical Practice, and local and institutional policies.
Maintain research quality.
Address patient safety and regulatory compliance.
Safeguard institutional integrity.

Responsibilities

Oversee the informed consent process.
Manage patient eligibility and screening.
Assess and manage patient toxicity.
Conduct in-services for nursing staff in treating clinics.
Plan patient recruitment strategies.
Manage the logistics of patient visits.
Coordinate the collection and handling of clinical samples.
Collect specimens as needed.
Enlist the support of necessary ancillary departments.
Coordinate the ordering of required supplies.
Prepare study tubes.
Collect source documentation.
Perform data entry and management for assigned studies.
Work with Clinical Research Associates to facilitate data collection for CRFs (case report forms) and/or eCRFs for trials as assigned.
Prepare for and participate in monitoring visits.
Facilitate pre-site meetings, site initiation meetings, and protocol start-up meetings.