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Temporary Nurse Consultant

Remote / Online - Candidates ideally in
Chapel Hill, Orange County, North Carolina, 27517, USA
Listing for: Inside Higher Ed
Part Time, Seasonal/Temporary, Remote/Work from Home position
Listed on 2026-02-08
Job specializations:
  • Nursing
    Healthcare Nursing
Salary/Wage Range or Industry Benchmark: 34.17 - 40.13 USD Hourly USD 34.17 40.13 HOUR
Job Description & How to Apply Below

Overview

Be a Tar Heel! A global higher education leader in innovative teaching, research and public service, the

Department LCCC - Clinical Trials - 426806

Career Area Research Professionals

Posting Open Date 02/02/2026

Final date to receive applications 02/09/2026

Position Type Temporary Staff (SHRA)

Position Title Temporary Nurse Consultant

Position Number

Vacancy S026819

Full-time/Part-time Part-Time Temporary

Hours Per Week 25

Work Schedule Monday – Friday, 8:30 AM – 5:00 PM

Position Location North Carolina, US

Hiring Range $34.17 - $40.13 per hour

Proposed Start Date 02/16/2026

Estimated Duration Of Appointment 6 months not to exceed 11 months

Be a Tar Heel!

A global higher education leader in innovative teaching, research and public service, the University of North Carolina at Chapel Hill consistently ranks as one of the nation’s top public universities
. Known for its beautiful campus, world-class medical care, commitment to the arts and top athletic programs, Carolina is an ideal place to teach, work and learn. One of the best college towns and best places to live in the United States, Chapel Hill has diverse social, cultural, recreation and professional opportunities that span the campus and community. University employees can choose from a wide range of professional training opportunities for career growth, skill development and lifelong learning and enjoy exclusive perks that include numerous retail and restaurant discounts, savings on local child care centers and special rates for performing arts events.

Primary

Purpose Of Organizational Unit

Our mission is to improve the health and well-being of North Carolinians and others whom we serve. We accomplish this by providing leadership and excellence in the interrelated areas of patient care, education and research.

Patient care:
We promote health and provide superb clinical care while maintaining our strong tradition of reaching underserved populations and reducing health disparities across North Carolina and beyond.

Education:

We prepare tomorrow`s healthcare professionals and biomedical researchers from all backgrounds by facilitating learning within innovative and integrated curricula and team-oriented interprofessional education to ensure a highly skilled workforce.

Research:
We develop and support a rich array of outstanding health sciences research programs, centers and resources. We provide infrastructure and opportunities for collaboration among disciplines throughout and beyond our university to support outstanding research. We foster programs in the areas of basic, translational, mechanistic and population research.

Position Summary

The purpose of this part-time temporary, remote position is to support UNC Cancer Care Triangle Locations in 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.

Key Responsibilities Include
  • Re-consent research participants by telephone
  • Support team lead
  • Assist with daily screening of new…
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