Nurse Consultant - Journey

Position Summary 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. 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 Minimum Education And Experience Requirements Licensed to practice as a Registered Nurse in the State of North Carolina and two years of experience in the area of specialization. Required Qualifications, Competencies, And Experience Knowledge of ICH GCP, Federal Regulations and Guidelines and ability to follow established regulations, procedures, and protocols Strong computer skills Ability to gather data and document procedures Ability to plan work and coordinate multiple projects Adequate social acumen and customer service skills Ability to communicate effectively and professionally verbally and in writing Ability to work on evenings, weekends and/or holidays occasionally required Preferred Qualifications, Competencies, And Experience Previous experience with therapeutic clinical research involving drugs and/or devices Experience in Phase I, II, and III clinical research Experience navigating medical records and data extraction SOCRA / ACRP Certification Previous study coordinator experience to include exposure to oncology clinical trials or directly related oncology study coordinator experience Required Licenses/Certifications Licensed to practice as a Registered Nurse in the State of North Carolina. Position/Schedule Requirements Clinic – UNCH or ACC, Evening work occasionally, Exposure to Bloodborne Pathogens, Exposure to Hazardous Materials, Laboratory, Overtime occasionally, Weekend work occasionally. Equal Opportunity Employer Statement The University is an equal opportunity employer and welcomes all to apply without regard to age, color, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex, or sexual orientation. We encourage all qualified applicants to apply, including protected veterans and individuals with disabilities. #J-18808-Ljbffr The University of North Carolina at Chapel Hill