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Temporary Study Coordinator

Job in Chapel Hill, Orange County, North Carolina, 27517, USA
Listing for: University of North Carolina at Chapel Hill
Part Time, Seasonal/Temporary position
Listed on 2026-02-09
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 34.84 - 37.29 USD Hourly USD 34.84 37.29 HOUR
Job Description & How to Apply Below

Overview

Department: LCCC - Clinical Trials - 426806

Career Area:
Research Professionals

Posting Open Date: 02/02/2026

Final date to receive applications: 02/05/2026

Position Type:
Temporary Staff (SHRA)

Position Title:

Temporary Study Coordinator

Position Number:

Vacancy : S026820

Full-time/Part-time:
Part-Time Temporary

Hours per week: 10

Work Schedule:

Monday – Friday, 8:30 AM – 5:00 PM

Position Location:

North Carolina, US

Hiring Range: $34.84 - $37.29 per hour

Proposed

Start Date:

02/09/2026

Estimated Duration of Appointment: 4 months or less

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

Reporting to the Clinical Operations Manager, this part-time, temporary study coordinator position plays a pivotal role in advancing cancer research and improving patient outcomes by facilitating the conduct of oncology clinical trials in compliance with federal regulations, Good Clinical Practice, and institutional policies. This position independently manages multiple complex trials throughout their life cycle, including activation, implementation, and closure, under the direction of a Clinical Operations Manager.

  • Being a resource for assigned studies
  • Assist with study training and education
  • Data entry
  • Map out study processes
  • Other duties as assigned

This position is integral to the mission of the UNC/LCCC Clinical Trials Office, maintaining research quality and safeguarding institutional integrity, and driving discoveries that shape the future of cancer care.

Minimum Education and Experience Requirements

Bachelor’s degree in a discipline related to the field assigned and one year of related training or experience; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions.

Management Preferences
  • Previous experience with therapeutic clinical research involving drugs and/or devices
  • Experience with direct patient contact in the hospital/clinic setting
  • Experience or familiarity with medical terminology
  • Demonstrated ability to operate at a high degree of independence
  • Demonstrated ability to coordinate studies of high complexity
Campus Security Authority Responsibilities

Not Applicable.

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