Data Coordinator

Posting Information

Posting Information

Department LCCC - Clinical Trials-426806 Career Area Research Professionals Is this an internal only recruitment? No Posting Open Date 10/14/2026 Application Deadline 10/28/2026 Position Type Permanent Staff (SHRA) Position Title Soc/Clin Research Assistant - Advanced Salary Grade Equivalent NC10 / GN10 Working Title Data Coordinator Position Number 00059669 Vacancy ID P021468 Full-time/Part-time Permanent/Time-Limited Full-Time Permanent If time-limited, estimated duration of appointment Hours per week 40 Work Schedule

Monday- Friday, 8:30AM - 5:00PM

Work Location CHAPEL HILL, NC Position Location North Carolina, US Hiring Range $55,886 - $65,000 Pay Band Information

To learn more about the pay band for this branch and role, please see the Career Banding rates spreadsheet.

Notice to Applicants

This position is not eligible for H-1B sponsorship.

Position Summary 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 for numerous retail, restaurant and performing arts discounts, savings on local child care centers and special rates on select campus events. UNC-Chapel Hill offers full-time employees a comprehensive benefits package, paid leave, and a variety of health, life and retirement plans and additional programs that support a healthy work/life balance.

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

This position plays a vital role in advancing cancer research and improving patient outcomes by supporting the accurate collection and abstraction of clinical data for oncology trials conducted in compliance with federal regulations, Good Clinical Practice, and institutional policies. The Data Coordinator independently oversees data related activities for multiple complex studies throughout their life cycle, including activation, implementation, monitoring, and closure, under the direction of a Clinical Operations Manager.

Key responsibilities include:

Abstraction of clinical information from medical records and source documents to meet protocol specific requirements

Collection and entry of study required data, ensuring completeness, accuracy, and timely submission

Ongoing data reconciliation and query resolution to ensure data integrity

Collaboration with study teams, regulatory staff, and clinical coordinators to support protocol compliance and patient safety

Compilation and maintenance of research patient records, ensuring adherence to documentation standards, data reporting timelines, and audit-readiness

This position is essential to the mission of the UNC/LCCC Clinical Trials Office, upholding research quality, supporting regulatory compliance, and safeguarding institutional integrity while contributing to discoveries that shape the future of cancer care.

Minimum Education and Experience Requirements

Bachelor's degree; 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 investigational drugs and/or devices, including exposure to Phase I-III oncology trials, and demonstrated knowledge of ICH GCP, federal regulations, and protocol driven procedures.
• Strong ability to navigate medical records and perform accurate, high-quality data abstraction, data collection, and data entry, with attention to detail and adherence to documentation standards.
• Previous data coordinator experience or equivalent oncology clinical research experience, supported by strong computer skills and the ability to gather data, document procedures, and contribute to reports, trainings, and SOP development.
• Demonstrated capacity to manage multiple concurrent projects, plan work effectively, meet strict data submission deadlines, and coordinate tasks across various phases of study activity.
• Excellent professional communication skills (written and verbal), customer service orientation, and ability to work collaboratively in a team environment, with flexibility to work occasional evenings, weekends, or holidays as required.

Required Licenses/Certifications Special Physical/Mental Requirements Campus Security Authority Responsibilities

Not Applicable.

Position/Schedule Requirements Evening work occasionally, Exposure to Bloodborne Pathogens, Exposure to Hazardous Materials, Laboratory, Overtime occasionally, Weekend work occasionally Special Instructions Quick Link https://unc.peopleadmin.com/postings/326986

Contact Information

Office of Human Resources Contact Information

If you experience any problems accessing the system or have questions about the application process, please contact the Office of Human Resources at (919) 843-2300 or send an email to employment@unc.edu

Please note: The Office of Human Resources will not be able to provide specific updates regarding position or application status.

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.

Applicant Documents

Required Documents

• Curriculum Vitae / Resume
• Cover Letter

Optional Documents

• List of References

Posting Supplemental Questions

Required fields are indicated with an asterisk (*).

• • Please select the response below that best describes your experience/education for the Social/Clinical Research Assistant position.

• Bachelor's, Master's, and/or Doctorate in any field.

• Associate's in any field and at least 2 years of experience.

• Combination of post-high school education and experience to equal at least 4 years of related experience (ex: 1 year towards a degree and 3 years of experience).

• High School diploma/GED and at least 4 years of related experience.

• Did not complete high school but have a combination of high school education and experience to equal 8 years. (ex. 3 years of high school and 5 years of experience).

• None of the above

• • Do you have knowledge of GCP and ICH Guidelines?

• Yes

• No

• • Describe your working knowledge and facility with information technology.

(Open Ended Question)

• • Do you have CCRP or CCRC Certification?
• yes
• no