Clinical Research Regulatory Coordinator-CEDAS

Posting Information Posting Information DepartmentGastroint Biology and Dis Ctr-429001Career AreaResearch ProfessionalsIs this an internal only recruitment?NoPosting Open Date 09/02/2026Application Deadline09/09/2026Position TypePermanent Staff (SHRA)Position TitleSoc/Clin Research Assistant - AdvancedSalary Grade EquivalentNC10 / GN10Working TitleClinical Research Regulatory Coordinator-CEDASPosition Number20073916Vacancy IDP021344Full-time/Part-time Permanent/Time-LimitedFull-Time PermanentIf time-limited, estimated duration of appointmentHours per week40Work ScheduleMonday-Friday 8am-5pm, other times as neededWork LocationCHAPEL HILL, NCPosition LocationNorth Carolina, USHiring Range$48,000-$66,000Pay Band InformationTo learn more about the pay band for this branch and role, please see the Career Banding rates spreadsheet.Notice to ApplicantsThis 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 UnitOur 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 SummaryThis position will serve as a Clinical Research Regulatory Coordinator within the Center for Gastrointestinal Biology and Disease. The Clinical Research Participant Regulatory Coordinator is responsible for research regulatory management for a variety of complex clinical research protocols, including leading efforts in creating, gathering, editing, compiling, and reporting regulatory information. The Clinical Research Regulatory Coordinator will analyze and reconcile information from various sources to complete various regulatory based tasks, such as Institutional Review Board submissions and applications management, creation and maintenance of regulatory files, and quality assurance activities.Minimum Education and Experience RequirementsBachelor’s degree; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions.Management PreferencesExperience independently coordinating clinical trials with direct experience in eRegulatory systems (Veeva SiteVault, Florence, etc.),Required Licenses/CertificationsSpecial Physical/Mental Requirements Campus Security Authority ResponsibilitiesNot Applicable.Position/Schedule RequirementsClinic – UNCH or ACC, Evening work occasionallySpecial InstructionsQuick Link Contact Information Office of Human Resources Contact InformationIf you experience any problems accessing the system or have questions about the application process, please contact the Office of Human Resources at View phone number on click.appcast.io or send an email to View email address on click.appcast.io note: The Office of Human Resources will not be able to provide specific updates regarding position or application status.Equal Opportunity Employer StatementThe 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.