RN Clinical Research Coordinator
:pointer-events-auto content-visibility:auto supports- content-visibility:auto : contain-intrinsic-size:auto_100lvh R6Vx5W_threadScrollVars scroll-mb- calc(var( scroll-root-safe-area-inset-bottom,0px)+var( thread-response-height scroll-mt- calc(var( header-height)+min(200px,max(70px,20svh " dir="auto" data-turn-id="request-WEB:af65416a-0362-4d51-bdec-737fc2ed9e51-22" data-testid="conversation-turn-2" data-scroll-anchor="false" data-turn="assistant"> RN Clinical Research Coordinator III Location: Asheville, NC 28806Schedule: Monday Friday 8:00 AM 5:00 PMJob Type: Permanent Full-TimeSalary Range: $70,000 $90,000 AnnuallyWe are seeking an experienced Registered Nurse Clinical Research Coordinator III to support oncology clinical trials in Asheville, North Carolina. This role is responsible for coordinating and managing Phase 1 3 clinical research studies under the supervision of the Principal Investigator while ensuring compliance with FDA, ICH/GCP, and IRB regulations. Key Responsibilities Coordinate patient care for oncology clinical research protocolsReview study protocols and ensure compliance with study requirementsScreen and assess patients based on inclusion/exclusion criteriaConduct informed consent discussions and maintain accurate study documentationMonitor, document, and report adverse events and safety concernsManage investigational products, study medications, and research specimensMaintain regulatory documents and support IRB submissionsEnsure data accuracy and integrity in EDC/CTMS systemsSupport monitoring visits, audits, and CAPA processesAssist with research budgets and billing compliance Requirements Active Registered Nurse (RN) LicenseASN or BSN requiredMinimum 2 years of nursing experience requiredOncology experience preferredClinical research experience strongly preferredKnowledge of FDA, ICH/GCP, and IRB regulationsExperience with EMR, EDC, and CTMS systems preferredStrong communication, organizational, and critical thinking skillsValid Driver s License required Preferred Skills Experience with Phase 1 3 clinical trialsAbility to work independently in a fast-paced multi-site environmentStrong attention to detail and documentation accuracy Additional Information Day Shift Full-TimeNo holiday coverage requiredState License: Upon AcceptanceBilingual not requiredIf you are interested or know someone who may be a good fit, please apply today.