Qureos

Find The RightJob.

UTS - Temporary Clinical Research Coordinator at UNC Chapel Hill

Posting Information

Department
HR UTS Partnership

Career Area
Research Professionals

Posting Open Date
04/24/2026

Application Deadline
05/01/2026

Position Type
Temporary Staff (SHRA)

Position Title
UTS - Temporary Clinical Research Coordinator at UNC Chapel Hill

Position Number

Vacancy ID
S027206

Full-time/Part-time
Full-Time Temporary

Hours per week

Work Schedule
Monday – Friday, 8am – 5pm, Onsite

Position Location

Hiring Range
$25.00 per hour

Proposed Start Date
12/01/2025

Estimated Duration of Appointment
6 months not to exceed 11 months

Position Information

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

Position Summary
The Research Assistant is responsible for supporting the lead coordinators in coordinating multiple complex trials through the protocol life cycles of activation, implementation and closure.

Research Study Execution
  • Collect study data through a variety of methods, per study protocol (e.g., administer surveys, observe/conduct study activities and record outcomes, electronic medical record data abstraction, biospecimens).
  • Perform clinical tests and procedures in accordance with the study protocol, following adequate training.
  • Record and organize study data and complete applicable case report forms (electronic or paper) as required in accordance with good clinical practice and ALCOA-C principles.
  • Manage study visits as applicable (e.g., schedule/coordinate visits, prepare materials, manage research charges, etc.)

Research- Subjects/Ethics
  • Maintain administrative study documentation (e.g., delegation of authority logs, training records)
  • Assist in the development and submission of regulatory applications and/or study materials (e.g., recruitment materials, informed consent forms)
  • Gather and store required regulatory documentation.
  • Prepare for study monitoring, participate in monitoring visits, and assist with corrections as applicable.
  • Track and document protocol deviations and adverse events.

Participant Management
  • Screen and recruit study participants for studies per study protocol and applicable standard operating procedures.
  • Obtain informed consent from study participants.

Research- Project Management
  • Participate in basic study start-up activities.
  • Participate in site initiation visits, study start-up meetings, and closeout visits for research studies.

Research- Quality Control
  • Ensure accuracy of data collected by conducting quality assurance/quality control procedures.
  • Report variations or discrepancies in data collected. Recognize discrepancies in patterns and make recommendations for process improvement.

Research- Lab Operations
  • Maintain study supplies (e.g., laboratory kits, administrative supplies).
  • Track and ship biospecimens, as applicable.

Minimum Education and Experience Requirements
  • One year of experience of patient facing clinical research experience



Management Preferences
  • Experience in clinical research
  • EPIC medical records experience


Special Physical/Mental Requirements

Campus Security Authority Responsibilities

© 2026 Qureos. All rights reserved.